US20100159223A1 - Modified perfluoropolymer sheet material and methods for making same - Google Patents

Modified perfluoropolymer sheet material and methods for making same Download PDF

Info

Publication number
US20100159223A1
US20100159223A1 US12/641,972 US64197209A US2010159223A1 US 20100159223 A1 US20100159223 A1 US 20100159223A1 US 64197209 A US64197209 A US 64197209A US 2010159223 A1 US2010159223 A1 US 2010159223A1
Authority
US
United States
Prior art keywords
coated fabric
coating
perfluoropolymer
sheet material
canceled
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US12/641,972
Other versions
US8969222B2 (en
Inventor
Frank M. Keese
Robert G. Pleydon
Anne B. Hardy
Hua Fan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Saint Gobain Performance Plastics Corp
Original Assignee
Saint Gobain Performance Plastics Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Saint Gobain Performance Plastics Corp filed Critical Saint Gobain Performance Plastics Corp
Priority to US12/641,972 priority Critical patent/US8969222B2/en
Assigned to SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION reassignment SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HARDY, ANNE B., KEESE, FRANK M., FAN, Hua, PLEYDON, ROBERT G.
Publication of US20100159223A1 publication Critical patent/US20100159223A1/en
Priority to US14/617,386 priority patent/US20150299943A1/en
Application granted granted Critical
Publication of US8969222B2 publication Critical patent/US8969222B2/en
Expired - Fee Related legal-status Critical Current
Adjusted expiration legal-status Critical

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N3/047Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with fluoropolymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B15/00Layered products comprising a layer of metal
    • B32B15/04Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/02Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
    • B32B5/022Non-woven fabric
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/02Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
    • B32B5/024Woven fabric
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/02Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
    • B32B5/08Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer the fibres or filaments of a layer being of different substances, e.g. conjugate fibres, mixture of different fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/22Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
    • B32B5/24Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
    • B32B5/26Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B9/00Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
    • B32B9/005Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00 comprising one layer of ceramic material, e.g. porcelain, ceramic tile
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D127/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
    • C09D127/18Homopolymers or copolymers of tetrafluoroethene
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/007Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
    • D06N3/0077Embossing; Pressing of the surface; Tumbling and crumbling; Cracking; Cooling; Heating, e.g. mirror finish
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/12Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
    • D06N3/128Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with silicon polymers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/18Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials
    • D06N3/183Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials the layers are one next to the other
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/18Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials
    • D06N3/186Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with two layers of different macromolecular materials one of the layers is on one surface of the fibrous web and the other layer is on the other surface of the fibrous web
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2255/00Coating on the layer surface
    • B32B2255/02Coating on the layer surface on fibrous or filamentary layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2255/00Coating on the layer surface
    • B32B2255/26Polymeric coating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/02Synthetic macromolecular fibres
    • B32B2262/0253Polyolefin fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/02Synthetic macromolecular fibres
    • B32B2262/0261Polyamide fibres
    • B32B2262/0269Aromatic polyamide fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/02Synthetic macromolecular fibres
    • B32B2262/0276Polyester fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/10Inorganic fibres
    • B32B2262/101Glass fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/10Inorganic fibres
    • B32B2262/106Carbon fibres, e.g. graphite fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2262/00Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
    • B32B2262/14Mixture of at least two fibres made of different materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00Properties of the layers or laminate
    • B32B2307/70Other properties
    • B32B2307/718Weight, e.g. weight per square meter
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/3154Of fluorinated addition polymer from unsaturated monomers
    • Y10T428/31544Addition polymer is perhalogenated
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2213Coating or impregnation is specified as weather proof, water vapor resistant, or moisture resistant
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/259Coating or impregnation provides protection from radiation [e.g., U.V., visible light, I.R., micscheme-change-itemave, high energy particle, etc.] or heat retention thru radiation absorption
    • Y10T442/2598Radiation reflective
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/273Coating or impregnation provides wear or abrasion resistance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2762Coated or impregnated natural fiber fabric [e.g., cotton, wool, silk, linen, etc.]
    • Y10T442/277Coated or impregnated cellulosic fiber fabric
    • Y10T442/2803Polymeric coating or impregnation from a silane or siloxane not specified as lubricant or water repellent
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2926Coated or impregnated inorganic fiber fabric
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T442/00Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
    • Y10T442/20Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
    • Y10T442/2926Coated or impregnated inorganic fiber fabric
    • Y10T442/2992Coated or impregnated glass fiber fabric

Definitions

  • This disclosure in general, relates to elastomer modified perfluoropolymer sheet materials.
  • Fabric reinforced polytetrafluoroethylene (PTFE) composites are employed in a variety of industries. In general, such composites are known to be resistant to the accumulation of dirt and grime and have a low coefficient of friction. However, conventional reinforced PTFE composites generally have a firm hand and drape. In other words, conventional reinforced PTFE composites are stiff and springy and cannot be formed into compound or double curve shapes without wrinkling or creasing. Furthermore, such conventional composites can have little sound dampening capability and can rattle and pop when deformed.
  • FIG. 1 , FIG. 2 , FIG. 3 , and FIG. 4 include illustrations of exemplary sheet materials.
  • FIG. 5 and FIG. 6 include illustrations of exemplary automobile HVAC systems.
  • the sheet material includes a blend of a perfluoropolymer and a silicone polymer.
  • the silicone polymer forms about 2 wt % to about 30 wt % of the blend.
  • the sheet material can include additional layers.
  • the sheet material can include a reinforcement layer.
  • the reinforcement layer can include a fibrous material, such as a PTFE coated fiberglass material.
  • the sheet material is a standalone sheet material without additional layers or reinforcement.
  • the sheet material can be formed by coating a carrier with a polymer dispersion.
  • the dispersion includes a perfluoropolymer and silicone polymer in an amount of 2% to 30% by weight based on the total weight of the solids in the dispersion.
  • the dispersion can be an aqueous dispersion.
  • the carrier includes a reinforcement material that is incorporated into the sheet material upon sintering or fusing of the coating.
  • the carrier is detachable from the sheet material formed of the coating material, resulting in a sheet material absent reinforcement.
  • the sheet material is a standalone sheet material absent reinforcement.
  • the sheet material 100 illustrated in FIG. 1 includes a layer 102 formed of a blend of perfluoropolymer and silicone polymer. As illustrated, the material 100 is free of reinforcement. Alternatively, additional layers can be disposed on either major surface of the layer 102 .
  • the blend includes a fluorinated polymer.
  • the fluorinated polymer can be a homopolymer of fluorine-substituted monomers or a copolymer including at least one fluorine-substituted monomer.
  • Exemplary fluorine substituted monomers include tetrafluoroethylene (TFE), vinylidene fluoride (VF2), hexafluoropropylene (HFP), chlorotrifluoroethylene (CTFE), perfluoroethylvinyl ether (PEVE), perfluoromethylvinyl ether (PMVE), and perfluoropropylvinyl ether (PPVE).
  • fluorinated polymers examples include polytetrafluoroethylene (PTFE), perfluoroalkylvinyl ether (PFA), fluorinated ethylene-propylene copolymer (FEP), ethylene tetrafluoroethylene copolymer (ETFE), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), and TFE copolymers with VF2 or HFP.
  • the blend includes a perfluoropolymer, such as PTFE, polyhexafluoropropylene (HFP), fluorinated ethylene propylene (FEP), perfluoroalkylvinyl (PFA), or any combination thereof.
  • the perfluoropolymer includes polytetrafluoroethylene (PTFE).
  • the perfluoropolymer is derived from a dispersion, such as an aqueous dispersion.
  • the silicone polymer can include a polysiloxane.
  • the silicone polymer can include a polyalkylsiloxane, a phenylsilicone, a fluorosilicone, or any combination thereof.
  • a polyalkysiloxane includes a polydimethylsiloxane, a polydipropylsiloxane, a polymethylpropylsiloxane, or any combination thereof.
  • the silicone polymer can be derived from an aqueous dispersion of precured silicone polymers.
  • the silicone polymer can be derived from an aqueous dispersion and can include precured silicone with terminal end groups that undergo condensation reaction during drying.
  • the silicone polymer can be derived from an aqueous dispersion of precured silicone with terminal groups or additives, such as cross-linkers, that undergo a condensation reaction when dried.
  • the silicone polymer can be selected from a silicone polymer dispersion available from Wacker-Chemie GmbH, Munchen, Germany, such as the Wacker CT27E silicone rubber dispersion, available from Dow Corning, such as Additive 84, or available from Shin Etsu, such as Polon MF 56.
  • the blend can include silicone polymer in an amount in a range of 2 wt % to 30 wt % based on the total weight of the fused blend.
  • the blend can include silicone polymer in an amount in a range of 5 wt % to 30 wt %, such as a range of 10 wt % to 30 wt %, or even a range of 15 wt % to 20 wt %.
  • the blend can include fluoropolymer, such as perfluoropolymer, in an amount in a range of 70 wt % to 98 wt %, such as a range of 75 wt % to 90 wt %, or even a range of 80 wt % to 85 wt %.
  • fluoropolymer such as perfluoropolymer
  • the blend can include fillers.
  • the blend can include fillers, light stabilizers, pigments, and bonding aids.
  • Exemplary fillers include talc, silica, and calcium carbonate.
  • Exemplary light absorbing additives and pigments include TiO 2 , Fe 2 O 3 , carbon black, and calcined mixed metal oxides.
  • Such fillers can be included in the blend in an amount not greater than 60 wt %, such as not greater than 40 wt %, not greater than 15 wt %, or even not greater than 5 wt %.
  • the sheet material can include a reinforcement.
  • a sheet material 200 includes a reinforcement layer 202 .
  • layer 204 can contact the reinforcement layer 202 directly without intervening layers, such as adhesive or surface treatment.
  • the reinforcement layer 202 can include a fibrous reinforcement, such as a woven or nonwoven fibrous reinforcement.
  • the fibrous reinforcement can be a woven fabric or an intermeshing of random fibrous strands.
  • the fabric is a woven glass fabric.
  • the reinforcement can include a mesh of ceramic, plastic, or metallic material or sheets of composite materials, among others.
  • the reinforcement layer 202 can take the form of a substrate, typically a sheet.
  • Embodiments can use supports formed of high melting point thermoplastics, such as thermoplastic polyimides, polyether-ether ketones, polyaryl ketones, polyphenylene sulfide, and polyetherimides; thermosetting plastics, particularly of the high temperature capable thermosetting resins, such as polyimides; coated or laminated textiles based on the above thermoplastics or similar thermally stable resins and thermally stable reinforcements such as fiberglass, graphite, and polyaramid; plastic coated metal foil; and metallized or metal foil laminated plastic films.
  • thermoplastic polyimides such as thermoplastic polyimides, polyether-ether ketones, polyaryl ketones, polyphenylene sulfide, and polyetherimides
  • thermosetting plastics particularly of the high temperature capable thermosetting resins, such as polyimides
  • coated or laminated textiles based on the above thermoplastics or similar thermally stable resins and thermally stable reinforcements such as fiberglass, graphite, and polyaramid
  • plastic coated metal foil such as aluminum foil
  • exemplary embodiments include woven and non-woven materials formed of fibers selected from aramid, fluorinated polymer, fiberglass, graphite, polyimide, polyphenylene sulfide, polyketones, polyesters, or a combination thereof.
  • the fibrous reinforcement includes a fiberglass reinforcement that has been cleaned or pretreated with heat.
  • the fibrous reinforcement can be a coated fiberglass reinforcement.
  • each of the fibers of the fiberglass can be individually coated with a polymeric coating, such as a fluoropolymer coating, for example, PTFE.
  • the layer 204 can include the blend described above in relation to layer 102 of FIG. 1 .
  • the layer 204 can be applied in an amount of at least 1.5 osy. Given that a woven fibrous reinforcement can undulate, the amount of the layer is provided in weight per area (ounces per square yard (osy)).
  • the layer can be applied in an amount of at least 1.8 osy, such as at least 2.0 osy, at least 4.0 osy, at least 4.5 osy, or even at least 6.0 osy.
  • the coating is applied in an amount not greater than 50 osy.
  • the blend of perfluoropolymer and silicone elastomer can be applied over a coated reinforcement.
  • a sheet material 300 can include a reinforcement layer 302 that is coated with layer 304 .
  • the layer 304 can be further coated with a layer 306 that includes a blend of perfluoropolymer and silicone polymer, such as the blend described above.
  • the reinforcement layer 302 can be a fibrous woven or nonwoven reinforcement material, as described above in relation to layer 202 of FIG. 2 .
  • the fibrous reinforcement can be coated with a layer of perfluoropolymer, such as PTFE, FEP, PFA, or any combination thereof.
  • the layer 304 can be applied in an amount of at least 0.5 osy.
  • the layer 304 can be applied in an amount in a range of 0.5 osy to 2.5 osy, such as 0.5 osy to 2.0 osy, 0.5 osy to 1.5 osy, or 0.5 osy to 1.0 osy.
  • the layer 306 can be applied over and disposed on the layer 304 .
  • the layer 306 can directly contact the layer 304 absent any intervening layers, such as adhesive or surface treatment.
  • the layer 306 includes a blend of perfluoropolymer and silicone polymer, such as the blend described above in relation to layer 102 of FIG. 1 .
  • the layer 306 is applied in an amount of at least 1.5 osy, such as at least 1.8 osy, or even at least 2.0 osy.
  • the layer 306 can be applied in an amount of at least 4.0 osy, such as at least 6.0 osy, but in each case, the amount of layer 306 is not greater than 50 osy.
  • a top coat can be applied over the blend.
  • a sheet material 400 illustrated in FIG. 4 can include a structure similar to that described in relation to FIG. 3 , including a reinforcement 402 coated with a perfluoropolymer layer 404 , which is in turn coated with a polymer blend layer 406 .
  • a further layer 408 can be applied over and disposed on the polymer blend layer 406 , for example, directly contacting layer 406 without intervening layers.
  • the additional layer 408 can be formed of a perfluoropolymer, such as PTFE, FEP, PFA, or any combination thereof.
  • the further layer 408 can be applied in an amount in a range of 0.5 osy to 2.5 osy, such as a range of 0.5 osy to 2.0 osy, a range of 0.5 osy to 1.5 osy, or a range of 0.5 osy to 1.0 osy.
  • the layer 408 can include a hard silicone coating, such as a silicone coating having a durometer of at least about 90 as measured on a Shore A scale, or at least about 20, as measured on a Shore D scale.
  • the layer 408 provides the surface of the sheet material 400 with desired non-tack and low friction properties.
  • the layer 408 can have hardness at least about 95, such as at least about 100 on the Shore A scale.
  • the layer 408 is relatively harder than the layer 406 .
  • hardness can be modified by, for example, modification of cross-link density, incorporation of fillers, or any combination thereof.
  • one or more additional layers can be provided which can impart surface functionality to the sheet material. While each of the above embodiments illustrated in FIGS. 2-4 are symmetric about the reinforcement layers, the layers can alternatively be applied in an asymmetric form, wherein one or more of the layers can be absent from one of the sides or each of the layers can be applied in different thicknesses on different sides.
  • the layers can be applied as fused layer or semifused layers. Semifused layers can be adhered to semifused layers of other films, substrates, fabrics, or sheets, and fused to bond the sheet material to the other material.
  • the total weight of the coated fabric can be at least 4.0 osy.
  • the total weight of the coated fabric can be at least 4.5 osy, such as at least 6.0 osy, or even at least 10 osy.
  • the fabric can have a total thickness of at least 3.5 mils, such as at least 5.0 mils, or even at least 9 mils.
  • the fabric has a total weight of not greater than 60 osy and a thickness not greater than 100 mils.
  • the sheet material exhibits a desirable stiffness and hand which remarkably exhibits near isotropy with respect to the machine direction and the cross direction.
  • the sheet material can exhibit a Gurley stiffness in the machine direction of not greater than 550.
  • the Gurley stiffness in the machine direction is not greater than 525, such as not greater than 500.
  • the Gurley stiffness is not greater than 800, such as not greater than 600, or even not greater than 500.
  • the coated fabric can have a Gurley Directional Ratio, defined as the ratio of the Gurley stiffness in the cross direction over the Gurley stiffness in the machine direction, of not greater than 1.3.
  • the Gurley Directional Ratio can be not greater than 1.1, such as not greater than 1.0.
  • the sheet material exhibits desirable trapezoidal tear strength in both the machine direction and the cross direction.
  • the trapezoidal tear strength in both the machine and cross directions is more closely matched.
  • the trapezoidal tear strength in the machine direction can be at least 13 lbs, such as at least 16 lbs, at least 22 lbs, or even at least 25 lbs.
  • the trapezoidal tear strength of the sheet material can be at least 11 lbs in the cross direction, such as at least 13 lbs, at least 16 lbs, or even at least 20 lbs.
  • Trapezoidal tear strength is measured in accordance with ASTM D751 as modified by D4969.
  • the Tear Directional Ratio defined as the ratio of the trapezoidal tear strength in the cross direction over the trapezoidal tear strength in the machine direction is at least 0.77.
  • the Tear Directional Ratio can be at least 0.81, such as at least 0.85.
  • the sheet material exhibits an unexpected and desirable change in Gurley stiffness or trapezoidal tear strength relative to fabrics of similar weight formed from similar reinforcement and PTFE alone.
  • the Gurley stiffness can be at least 10% less than a PTFE coated fabric, such as at least 18% less, at least 25% less, or even at least 30% less.
  • the percent decrease in Gurley stiffness relative to the reinforcement coated with PTFE alone is defined as the Gurley Index.
  • the trapezoidal tear strength can be at least 25% more than a PTFE coated fabric, such as at least 50% more, at least 70% more, or even at least 90% more.
  • the increase in trapezoidal tear strength relative to the reinforcement coated with PTFE alone is defined as the Tear Index.
  • the sheet material can exhibit a specular reflectance of not greater than 0.5%, such as not greater than 0.2%, as measured in accordance with ASTM E424.
  • the surface can have a coefficient to friction of not greater than 0.2.
  • the sheet material can provide a cohesive structure that has a desirable coating adhesion as determined by ASTM D4851-88 modified by heating and pressing for as much as 2 minutes to form test samples and performing tests on samples 1′′ in width.
  • the coating adhesion can be at least 1.8 lbs/in, such as at least 2.0 lb/in, at least 2.5 lb/in, at least 3.0 lb/in, at least 3.5 lb/in, at least 4.0 lb/in, or even at least 4.5 lb/in.
  • the sheet material can have a warp break strength (break strength in the machine direction) of at least 270 lb/in, such as at least 290 lb/in, at least 300 lb/in, or even at least 350 lb/in.
  • the sheet material exhibits a desirable fill break strength (break strength in the cross direction) of at least 200 lb/in, such as at least 230 lb/in, at least 250 lb/in, or even at least 270 lb/in. Strength is determined in accordance with ASTM D3751.
  • the sheet material exhibits improved break strength in the warp or machine direction relative to a comparable sheet material formed of a similar reinforcement and coated with an equivalent thickness of perfluoropolymer, such as PTFE.
  • the Warp Strength Index defined as the percent increase in warp break strength relative to the comparable sheet material, is at least 8%, such as at least 10%, at least 12%, or even at least 15%.
  • the sheet material exhibits desirable retention of break strength when stressed through creasing or folding. Based on the Flex Fold test according to ASTM D3751 using a 10 lb roller, the sheet material retains a percentage of its warp break strength.
  • the sheet material can exhibits a Strength Retention, defined as the warp break strength retained by a sample after undergoing a Flex Fold test expressed as a percentage of the original warp break strength prior to flexing, of at least 25%, such as at least 35%, or even at least 40%.
  • the sheet material also exhibits a desirable combination of cohesion and break strength.
  • the sheet material can exhibit both improved break strength and coating adhesion.
  • the sheet material can exhibit a Cohesive Ratio, defined as the warp break strength divided by the coating adhesion, of not greater than 142.5, such as not greater than 100, not greater than 85, or even not greater than 75.
  • the sheet material exhibits low permeability.
  • the sheet material is not porous or layers that may be porous, such as a layer comprising the perfluoropolymer/silicone blend, include pores that are not substantially interconnected or are localized to that layer.
  • the sheet material can have a permeability of not greater than 0.001 cuin/min, as measured in accordance with ASTM D737, such as having a permeability of approximately 0 cuin/min within the sensitivity of the measuring device.
  • ASTM D737 such as having a permeability of approximately 0 cuin/min within the sensitivity of the measuring device.
  • the sheet material can be impermeable.
  • a sheet material including a reinforcement layer and a layer comprising the fluoropolymer/silicone blend described above has a permeability of not greater than 0.001 cuin/min.
  • the sheet material exhibits low permeability when exposed to hydrocarbons and solvent.
  • VTR vapor transmission rate
  • the vapor transmission rate (VTR) permeation when measured in accordance with ASTM D814 under exposure to Fuel B is not greater than 2.0 mg/s*m 2 , such as not greater than 1.5 mg/s*m 2 , not greater than 1.0 mg/s*m 2 , not greater than 0.5 mg/s*m 2 , or even not greater than 0.3 mg/s*m 2 .
  • a dispersion can be prepared including a blend of perfluoropolymer particles and precured silicone elastomer particles.
  • the dispersion can be an aqueous dispersion.
  • a dispersion of perfluoropolymer, such as PTFE is mixed with a dispersion of precured silicone polymer.
  • the silicone polymer can form between 2 wt % and 30 wt % based on the solids of the dispersion.
  • the silicone polymer can form 5 wt % to 30 wt % of the solids of the dispersions, such as 10 wt % to 30 wt %, 10 wt % to 25 wt %, or even 15 wt % to 20 wt % of the solids of the dispersion.
  • the perfluoropolymer can form the remainder of the solids of the dispersion.
  • the perfluoropolymer can form 70 wt % to 98 wt % of the solid content of the dispersion, such as 75 wt % to 90 wt % or even 80 wt % to 85 wt % of the solid content of the dispersion.
  • a solid filler can be included in the dispersion.
  • the solid filler can form not greater than 60 wt % of the solids in the dispersion, such as not greater than 40 wt %, not greater than 15 wt %, or not greater than 5 wt %.
  • a carrier can be coated with the dispersion through a process, such as dip coating, knife coating, or casting. Excess material can be wiped and the coating dried and sintered or fused.
  • the carrier can be a solid material that can be separable from the sheet material.
  • the sheet material including a layer of the blend can be formed by first coating the carrier, drying and sintering the material, and separating the material from the carrier to form a sheet material.
  • the sheet material is free of a reinforcement layer.
  • the carrier can be a reinforcement material, which can be coated with the dispersion.
  • the reinforcement material can be a fibrous reinforcement and in particular, can be a coated fibrous reinforcement.
  • the fibrous reinforcement such as a fiberglass, can be drawn through an aqueous dispersion.
  • the aqueous dispersion can be a dispersion of perfluoropolymer absent the silicone.
  • the reinforcement material can be drawn through an aqueous dispersion of PTFE.
  • the fibrous reinforcement coated with the aqueous dispersion is passed through a wiping arrangement to remove excess perfluoropolymer dispersion and is passed through an oven.
  • the oven can be, for example, a three zone tower oven.
  • the three zone tower oven can fuse the coated material.
  • the first zone can dry the dispersion at a temperature in a range of 200° F. to 300° F.
  • the second zone can heat the deposited perfluoropolymer to remove surfactants and other additives.
  • the second zone can heat the deposited perfluoropolymer at a temperature in a range of 500° F. to 600° F.
  • the third zone can melt, sinter, or fuse the perfluoropolymer.
  • the third zone can fuse the perfluoropolymer at a temperature in the range of 680° F. to 700° F.
  • the three zone tower can be set to semifuse the coated material.
  • the first zone can dry the dispersion at a temperature in a range of 200° F. to 300° F.
  • the second zone can heat the deposited perfluoropolymer to remove surfactants and other additives.
  • the second zone can heat the deposited perfluoropolymer at a temperature in a range of 500° F. to 600° F.
  • the third zone can be set to a temperature lower than the melting point of the perfluoropolymer.
  • the third zone can be set to a temperature in the range of 550° F. to 600° F.
  • the process can be repeated.
  • the fibrous reinforcement such as an uncoated fibrous reinforcement or the coated fibrous reinforcement
  • the fibrous reinforcement can be drawn through a bath of aqueous dispersion including the blend of perfluoropolymer and silicone elastomer.
  • Excess dispersion can be removed using a wiping arrangement, such as a metering bar, a Bird bar, a wire-wound metering bar, a K bar, or other similar equipment or combinations thereof.
  • the reinforcement material coated with the blended dispersion is heated.
  • the dispersion can be heated to dry the dispersion, remove surfactants or other additives and subsequently to melt the perfluoropolymer and cure the precured silicone polymer.
  • the coated reinforcement material can pass through a three zone tower oven, including a first zone that dries the dispersion at a temperature in a range of 200° F. to 300° F.
  • a second zone of the oven can remove surfactants and other additives from the deposited blend coating at a temperature in a range of 500° F. to 600° F.
  • the third zone can be set to fuse the blend, for example, melt the perfluoropolymer, or can be set to form a semifused layer.
  • the third zone can be set to a temperature in a range of 680° F. to 700° F. to fuse the material.
  • the third zone can be set to a temperature in a range of 550° F. to 600° F. to semifuse the layer.
  • the coating can be heating in an oven including one zone, two zones, or more.
  • the coating can be dried and sintered in two stages.
  • the sheet material can be pressed or calendered.
  • the drums of the calender can be set to a temperature in a range of 275° F. to 400° F. and to a pressure between the drums in a range of 500 psi to 4000 psi.
  • the calendered sheet material including the semifused layer or layers can be subjected to fusing conditions, such as a temperature within a range of 680° F. to 700° F.
  • the sheet material can pass through a cooling plenum from which it can be directed to a subsequent dip pan to begin formation of a further layer of film, to a stripping apparatus, or to a roll for storage.
  • sheets of composite material are formed and subsequently layered over the reinforcement material. These sheets can be further processed to bond to the reinforcement material.
  • sheets of material can be laminated to the reinforcement material.
  • a reinforcement material can be passed through an emulsion of perfluoropolymer, such as PTFE, and fused.
  • the reinforcement material can be passed through the emulsion once.
  • the reinforcement material can be passed through a second time, or optionally a third time, and fused. Each pass results in additional thickness referred to herein as a pass.
  • the sheet material can be passed through an emulsion including a blend of perfluoropolymer and silicone. The sheet material can be passed through the emulsion of the blend at least once.
  • the sheet material can be passed through the emulsion of the blend twice or can be passed through the emulsion three or more times.
  • the blend layer can be fused.
  • the blend layer can be semifused, as described above, and can be calendered, pressed, or further treated, and subsequently fused.
  • additional layers can be applied.
  • an additional layer or layers can be coated on the sheet material by passing the sheet material through an additional emulsion.
  • the additional emulsion can be a perfluoropolymer emulsion.
  • the additional emulsion can be a silicone emulsion. Passes underlying the additional layers can be fused or semifused when the additional layer is coated.
  • the additional layer or layers can be fused, or can be semifused.
  • the additional layer or layers can be calendered or otherwise treated.
  • a semifused layer either the blend layer or an additional layer can be pressed into contact with another semifused layer of another sheet material or film.
  • the construct can be fused to bond the sheet materials or sheet material and film together.
  • an additional semifused PTFE outer layer can be pressed or calendered into contact with a semifused PTFE layer of a second sheet material or film and subsequently fused.
  • a semifused blend layer can be placed in contact with a semifused blend layer or semifused perfluoropolymer layer of a second sheet material or film, and subsequently fused.
  • the sheet material includes a reinforcement material coated with a single pass of perfluoropolymer, such as PTFE, that is coated with at least one pass and likely two passes of a blend.
  • a reinforcement material coated with a single pass of perfluoropolymer such as PTFE
  • the passes of the blend can be semifused, calendered, and subsequently, fused.
  • the sheet material includes the reinforcement material, a pass of fused perfluoropolymer, two passes of fused blend, and an outer layer formed of at least one pass of a polymer, such as a perfluoropolymer or a silicone polymer.
  • the outer layer is fused.
  • the outer layer is semifused.
  • an outer layer that is semifused or a blend layer that is semifused can be placed in contact with a film, such as a film including perfluoropolymer or silicone.
  • a film such as a film including perfluoropolymer or silicone.
  • the film is a defect free perfluoropolymer film, such as a PTFE film.
  • a film has a more uniform consistency than a coating and lower variability in properties.
  • An example of a film includes a skived film, a cast film, or an extruded film.
  • the dispersion including the blend of perfluoropolymer and silicone polymer permits thicker coatings to be applied in a single pass.
  • a dispersion of the blend in a single pass, can be coated to form a coating having a weight of at least 1.5 osy, such as at least 1.8 osy, at least 2.0 osy, or even at least 2.4 osy.
  • coatings of PTFE when coated to form layers of weight greater than 1.0 osy form cracks, deformations or surface irregularities unless the coating is performed in multiple passes.
  • a sheet material 502 formed as described above can be particularly well suited as a film valve.
  • the film valve can extend between rollers 504 .
  • a film valve 502 can be drawn between rollers 504 to align holes 608 , 610 , and 612 as illustrated at FIG. 6 with vents 508 .
  • a source of air such as a fan, can direct air through the film valve 502 and into one or more of the vents 508 .
  • embodiments of the sheet material described above exhibit desirable flexibility and hand as well as other desirable features which make the sheet material particularly well suited for use in automobile HVAC systems.
  • embodiments of the sheet material have greater sound absorption than a PTFE coated fabric having the same reinforcement.
  • the sheet material exhibits desirable properties, including breaking strength and crease and tear strength resistance, as well as, conformability, which enhance the useful life of the material.
  • the sheet material is particularly suited for use as a high temperature release sheet or as a belt in industrial applications.
  • the release fabric (whether in sheet or belt form) is forced to conform somewhat to the irregular contours of the photovoltaic cell through vacuum or mechanical pressure.
  • Such forced conformation can cause the photovoltaic material to distort, which can cause creases that lead to defects in the photovoltaic cells being produced.
  • the conventional material can be severely weakened after repeated pressing cycles and can fail to due breaking or tearing.
  • the present sheet material withstands repeated press cycles until loss of release properties, and not from mechanical failure. The enhanced physical properties allow the release fabric to remain in place longer, reducing the number of change outs due to premature failure.
  • release applications rely on the physical properties of the reinforcing material as much as the non-stick property of the perfluoropolymer.
  • Such applications include other laminating or pressing operations in textiles, automotive and general industrial applications.
  • Sealing of plastic packaging, whether rigid shapes like battery packages or thin flexible films that encase toilet paper and paper towels benefit from the high improved tensile strength, higher crease and tear resistance strength as well as the improved conformability of the present sheet material, as the release sheets and belting products through which heat is applied to form or seal these materials conform to irregular shapes and materials of various hardness (i.e., the core in the toilet paper or paper towel relative to the toilet paper itself).
  • adhesive backed pressure sensitive tape products are used in similar applications, and often conform to irregular heat sealing jaws, wires or molds.
  • the present sheet material is useful in applications where the release fabric or tape is not kept in a planar shape. In such applications, the present sheet material exhibits increased useful release life.
  • the present sheet material can be useful in insulator jacketing, bladder applications, expansion joints, HVAC control films, photovoltaic release sheets, and floating roof seals.
  • Embodiments including food grade silicone can also be used in the food and food services industries, for example, as spill mats or industrial cooking belts, among other food preparation apparatuses.
  • the coated fabric is passed through a wiping arrangement to remove excess PTFE dispersion and is passed through a three-zone tower oven, which in the first zone dries the dispersion at a temperature in a range of 200° F. to 300° F., in the second zone heats the deposited PTFE resin at a temperature in a range of 500° F. to 600° F., and in the third zone melts the PTFE at a temperature in a range of 680° F. to 700° F.
  • the coated fabric weighs about 2.02 osy.
  • a second coating from a dispersion mixture of the DuPont TE-3859 PTFE dispersion and a silicone rubber dispersion, Wacker Silicones Finish CT27E (Wacker Silicones, Adrian, Mich.) is coated on to the coated fabric by drawing the coated fabric through the dispersion and wiping excess dispersion from the coated fabric.
  • the dispersion mixture is made by combining by simple stirring about 131 parts by weight (pbw) of the DuPont TE-3859 with about 31 pbw of the Wacker CT27E. The mixture is not reduced with water.
  • the coating comprising about 80 weight percent of PTFE and 20 weight percent of silicone rubber, is applied using the process described above, except that the wiping arrangement was modified to allow a greater weight of the coating formulation to be applied.
  • the subsequent total weight of the coated fabric is 4.24 osy and is 0.0035 inches thick.
  • a second sample is prepared using a similar, two-step process, with an industry style 2116 fiberglass fabric, greige finish, weighing after heat cleaning 3.13 osy, with 3.7 mils thick.
  • the intermediate PTFE-coated fabric weighs about 3.79 osy and the finished product weighs about 6.24 osy.
  • the finished product is about 0.0052 inches thick.
  • the two samples are measured for finished thickness, finished weight, and coefficient of friction.
  • the two samples are tested for break strength, load, trapezoidal tear strength, and coating adhesion, as illustrated in Table 1.
  • Example 1 An additional sample is prepared using the method described in Example 1.
  • the base fabric is an industrial style 7628 fiberglass fabric having a standard weight of 5.94 osy after cleaning.
  • An initial coating of PTFE is applied as described in relation to Example 1.
  • the blend coating composition described above is applied in three passes.
  • the weight of the fabric prior to application of the blend coating is 7.3 osy and following each of the three passes is 9.06 osy, 11.57 osy, and 12.39 osy, respectively.
  • the final thickness of the film is 0.0103 in.
  • sample 3 is compared to a standard 10 mil PTFE film (PTFE CF210) based on the same base fabric.
  • the sample and comparative sample are tested for Gurley stiffness, trapezoidal tear strength (ASTM D751), and specular reflectance (ASTM E424).
  • the blend sample exhibits a lower difference between stiffness in machine versus cross directions.
  • the Gurley Directional Ratio is less than 1.0, i.e., 0.97
  • the comparative sample exhibits a Gurley Directional Ratio significantly greater than 1.0.
  • the tear strength of the sample is higher than that of the comparative sample and the ratio between the directions is closer to 1.
  • the specular reflectance of the blend sample is lower. Additional coatings can be used to manipulate the reflectance.
  • Samples and comparative samples are prepared using an industrial standard 1528 fiberglass fabric. The samples are coated in passes that are fused. The samples and comparative samples are tested for mechanical properties, including machine direction trapezoidal tear strength, cross direction trapezoidal tear strength, warp (machine direction) break strength, fill (cross direction) break strength, strength retention, and coating adhesion.
  • Comparative samples are prepared by repeated passes of the 1528 fiberglass fabric through a PTFE emulsion to form a sheet material having a weight of 13.5 osy. The PTFE coating is fused.
  • a first sample (Sample 4) is prepared by applying a single fused pass of clear PTFE to the 1528 fiberglass fabric, followed by two semifused passes of a blend of PTFE and 20 wt % silicone, formed as describe in relation to Example 1. After application of the semifused passes, the blend layer is fused. A single pass of fused PTFE is applied over the blend layer.
  • a second sample (Sample 5) includes the 1528 fiberglass fabric and a pass of fused clear PTFE, coated with three passes of semifused blend including 10% silicone. The semifused passes are fused to form a blend layer that is subsequently coated with a fused clear PTFE layer.
  • a third sample (Sample 6) includes the 1528 fiberglass fabric and two passes of fused clear PTFE, coated with two passes of semifused blend including 20% silicone. The semifused passes are calendered and fused to form a blend layer that is subsequently coated with a fused clear PTFE layer.
  • a fourth sample (Sample 7) includes the 1528 fiberglass fabric and two passes of fused clear PTFE, coated with two passes of semifused blend including 20% silicone. The semifused passes are calendered and fused to form a blend layer that is subsequently coated with a fused clear PTFE layer. The sample is further subjected to an additional calendering.
  • a fifth sample includes the 1528 fiberglass fabric and a single pass of fused clear PTFE, coated with two passes of semifused blend including 20% silicone.
  • the semifused passes are coated with a semifused clear PTFE layer.
  • the material is subjected to calendering, followed by fusing.
  • An additional clear PTFE pass is fused to the material.
  • Table 3 illustrates the weight and mechanical properties of the samples and comparative samples. As illustrated, the samples exhibit desirable improvement in break strength. In addition, the samples exhibit a desirable Cohesion Ratio and Strength Retention.
  • Samples and comparative samples are prepared using an industrial standard 7628 fiberglass fabric. The samples are coated in passes that are fused. The samples and comparative samples are tested for mechanical properties, including machine direction trapezoidal tear strength, cross direction trapezoidal tear strength, warp (machine direction) break strength, fill (cross direction) break strength, strength retention, and coating adhesion.
  • Comparative samples (Comparative Samples 3 and 4) are prepared by repeated passes of the 7628 fiberglass fabric through a PTFE emulsion to form a sheet material having a weight of 12.7 osy. The PTFE coating is fused.
  • a first sample (Sample 9) is prepared by applying two pass of clear PTFE that are fused to the 7628 fiberglass fabric, followed by three semifused passes of a blend of PTFE and 20 wt % silicone. After application of the semifused passes, the blend layer is fused. A single pass of fused PTFE is applied over the blend layer.
  • a second sample (Sample 10) includes the 7628 fiberglass fabric and a pass of fused clear PTFE, coated with two passes of semifused blend including 20 wt % silicone.
  • the semifused passes coated with a semifused clear PTFE layer and calendered.
  • the calendered sheet material is fused, followed the application of a fused clear PTFE pass.
  • Table 4 illustrates the weight and mechanical properties of the samples and comparative samples. As illustrated, the samples exhibit a desirable break strength and desirable Strength Retention and Cohesion Ratio.
  • Samples are prepared using a 7628 fiberglass fabric or a 1564 fiberglass fabric.
  • a clear PTFE coating is applied and fused, followed by a single pass coating of a blend including 20 wt % silicone and PTFE, which is semifused.
  • a 1 mil PTFE film is laminated to the semifused blend layer and the construction is fused.
  • Samples are prepared using a 7628 fiberglass fabric or a 1528 fiberglass fabric.
  • a clear PTFE coating is applied and fused, followed by two pass coating of a blend either including 5 wt % or 10 wt % silicone and PTFE, which is subsequently fused.
  • a pass of clear PTFE is applied on the blend layer and fused.
  • Samples are formed in accordance with Example 5.
  • Sample 11 includes a 7628 greige fiberglass fabric
  • Sample 12 includes a 1564 greige fiberglass fabric. Properties of the samples are compared with those of CPI-10 42.5′′ (C5) and CPI-18 42.5′′ (C6), both available from Saint-Gobain. Table 5 illustrates the properties.
  • Samples 11 and 12 exhibit low permeation when exposed to Fuel B.
  • Samples 11 and 12 exhibit desirable mechanical properties relative to the comparative samples.
  • a coated fabric in a particular embodiment, includes a reinforcement, a first coating disposed on the reinforcement, and a second coating disposed on the first coating.
  • the first coating includes perfluoropolymer.
  • the second coating includes perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %. In an example, the range of silicone polymer is 10 wt % to 25 wt %, such as 15 wt % to 20 wt %.
  • the coated fabric can include a third coating on the second coating.
  • the third coating can include a fluoropolymer, such as a perfluoropolymer.
  • the third coating can include silicone.
  • the coated fabric has a Gurley stiffness in the machine direction of not greater than 550, such as not greater than 525, or not greater than 500.
  • the coated fabric has a Gurley stiffness in the cross direction of not greater than 800, such as not greater than 600, or not greater than 500.
  • the coated fabric can have a Gurley Directional Ratio of not greater than 1.3, such as not greater than 1.1, or not greater than 1.0.
  • the coated fabric has a trapezoidal tear strength in the machine direction of at least 13 lbs, such as at least 16 lbs, at least 20 lbs, at least 22 lbs, or at least 25 lbs.
  • the coated fabric has a trapezoidal tear strength in the cross direction of at least 11 lbs, such as at least 13 lbs, at least 16 lbs, or at least 20 lbs.
  • the coated fabric can have a Tear Directional Ratio of at least 0.77, such as at least 0.81, or at least 0.85. Further, the coated fabric can exhibit a Tear Index of at least 25%.
  • the coated fabric has a specular reflectance of not greater than 0.5%, such as not greater than 0.2%. Further, the coated fabric can have a coefficient of friction of not greater than 0.2. In addition, the coated fabric can have a coating adhesion of at least 1.8 lb/in, such as at least 2.0 lb/in, or at least 2.5 lb/in.
  • the coated fabric can have a warp break strength of at least 270 lb/in, such as at least 290 lb/in. Further, the fill break strength can be at least 200 lb/in.
  • the coated fabric can exhibit a Strength Retention of at least 25%, such as at least 35%.
  • the coated fabric can exhibit a Cohesion Ratio of not greater than 142.5, such as not greater than 100.
  • the perfluoropolymer includes PTFE, HFP, FEP, PFA, or a combination thereof.
  • the perfluoropolymer includes polytetrafluoroethylene.
  • the silicone polymer is derived from a precured silicone polymer dispersion, such as a condensation polymerized silicone.
  • the first coating is applied in an amount of at least 0.5 osy.
  • the second coating is applied in an amount of at least 1.5 osy, such as at least 1.8 osy, at least 2.0 osy, or at least 2.4 osy.
  • the total weight of the coated fabric can be at least 4.0 osy, such as at least 4.5 osy, or at least 6.0 osy.
  • a sheet material in another embodiment, includes a blend of perfluoropolymer and silicone polymer.
  • the blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the sheet material has a Gurley Directional Ratio of not greater than 1.3.
  • a sheet material includes a blend of perfluoropolymer and silicone polymer.
  • the blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the sheet material has a Tear Directional Ratio of at least 0.77.
  • a sheet material includes a blend of perfluoropolymer and silicone polymer.
  • the blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the sheet material has a total thickness of at least 9 mils and a Gurley stiffness of not greater than 550.
  • a venting system in another embodiment, includes a plurality of conduits, each having an opening, and includes a film having a plurality of openings.
  • the film is movable to align at least one opening with an opening of at least one of the conduit of the plurality of conduits.
  • the film includes a blend of perfluoropolymer and silicone polymer. The blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • a method of forming a sheet material includes coating a reinforcement with a first coating comprising a perfluoropolymer to form a first intermediate article, coating the first intermediate article with a second coating comprising a polymer dispersion to form a second intermediate article, and sintering the second intermediate article.
  • the polymer dispersion includes a perfluoropolymer and a silicone polymer.
  • the dispersion includes the silicone polymer in an amount in a range of 2 wt % to 30 wt % based on the total weight of solids in the polymer dispersion.
  • coating the first intermediate article with the second coating includes coating the first intermediate article with at least 2.0 osy of the second coating in a single step. In a further example, coating the first intermediate article with the second coating includes coating the first intermediate article with at least 2.4 osy of the second coating in a single step.
  • a method of forming a sheet material includes coating a carrier with at least 2.0 osy of a polymer dispersion comprising a perfluoropolymer and a silicone polymer.
  • the silicone polymer forms 2 wt % to 30 wt % of the solids content of the dispersion.
  • the method further includes drying the polymer dispersion and sintering the dried polymer dispersion.
  • the carrier forms a carrier web reinforcement that is incorporated into the sheet material.
  • the carrier comprises a fibrous reinforcement material.
  • the carrier includes a fibrous reinforcement material coated with a perfluoropolymer.
  • the carrier is a support separable from the coating and the method further includes delaminating the coating from the carrier.
  • a sheet material includes a polymer blend comprising perfluoropolymer and silicone polymer.
  • the polymer blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the sheet material further includes a reinforcement layer, the polymer blend disposed on the reinforcement layer.
  • the reinforcement layer comprises a fibrous reinforcement material.
  • the reinforcement layer can include a fibrous reinforcement material coated with a perfluoropolymer.
  • a coated fabric in a further embodiment, includes a reinforcement material; and a coating overlying the reinforcement material.
  • the coating includes perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the coated fabric has a permeability of not greater than 0.001 cuin/min. In an example, the coated fabric is substantially impermeable.
  • the range of silicone polymer is 10 wt % to 25 wt %, such as 15 wt % to 20 wt %.
  • the coated fabric has a trapezoidal tear strength in the machine direction of at least 13 lbs.
  • the coated fabric has a coating adhesion of at least 1.8 lb/in.
  • the coated fabric exhibits a Strength Retention of at least 25%.
  • the perfluoropolymer includes polytetrafluoroethylene (PTFE), hexafluoropropylene (HFP), fluorinated ethylene propylene (FEP), perfluoroalkyl vinyl ether (PFA), a combination thereof.
  • PTFE polytetrafluoroethylene
  • HFP hexafluoropropylene
  • FEP fluorinated ethylene propylene
  • PFA perfluoroalkyl vinyl ether
  • the perfluoropolymer includes polytetrafluoroethylene (PTFE).
  • the silicone polymer can be derived from a precured silicone polymer dispersion.
  • the silicone can be a condensation polymerized silicone.
  • a sheet material in another embodiment, includes a single layer.
  • the single layer includes a polymer blend comprising perfluoropolymer and silicone polymer.
  • the polymer blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • a method of forming a coated fabric includes dispensing a fabric and applying a first emulsion coating to the fabric.
  • the first emulsion includes a perfluoropolymer.
  • the method also includes fusing the first emulsion coating to form a first layer and applying a second emulsion coating on the first emulsion coating.
  • the second emulsion coating includes a blend of perfluoropolymer and silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • the method further includes fusing the second emulsion coating to form a second layer.
  • the method further includes semifusing the second emulsion coating following applying the second emulsion coating and prior to fusing the second emulsion coating.
  • the method can further include calendering the second emulsion coating following semifusing the second emulsion coating.
  • the method can include contacting the second emulsion coating with a perfluoropolymer film following semifusing the second emulsion coating, wherein fusing the second emulsion coating includes fusing the second emulsion coating while in contact with the perfluoropolymer film.
  • the method further includes applying a third emulsion coating on the second emulsion coating.
  • the third emulsion coating includes a perfluoropolymer.
  • the third emulsion coating includes silicone.
  • the method can include semifusing the third emulsion coating, contacting the third emulsion coating with a film, and fusing the third emulsion coating while in contact with the film.
  • the method can also include semifusing the third emulsion coating, calendering the third emulsion coating, and fusing the third emulsion coating.
  • applying the third emulsion coating can include applying the third emulsion coating to the second emulsion coating while the second emulsion coating is in a semifused state.
  • the terms “over” or “overlie,” when used in relation to location indicate a location relatively closer to an outer surface of the sheet material when moving away from reinforcement material, if any.
  • the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion.
  • a process, method, article, or apparatus that comprises a list of features is not necessarily limited only to those features but may include other features not expressly listed or inherent to such process, method, article, or apparatus.
  • “or” refers to an inclusive-or and not to an exclusive-or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).

Abstract

A coated fabric includes a reinforcement, a first coating disposed on the reinforcement, and a second coating disposed on the first coating. The first coating includes perfluoropolymer. The second coating includes perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %.

Description

    CROSS-REFERENCE TO RELATED APPLICATION(S)
  • The present application claims priority from U.S. Provisional Patent Application No. 61/139,946, filed Dec. 22, 2008, entitled “MODIFIED PERFLUOROPOLYMER SHEET MATERIAL AND METHODS FOR MAKING SAME,” naming inventors Frank M. Keese and Robert G. Pleydon and claims priority from U.S. Provisional Patent Application No. 61/243,926, filed Sep. 18, 2009, entitled “MODIFIED PERFLUOROPOLYMER SHEET MATERIAL AND METHODS FOR MAKING SAME,” naming inventors Frank M. Keese, Robert G. Pleydon, Anne B. Hardy, and Hua Fan, which applications are incorporated by reference herein in their entirety.
  • FIELD OF THE DISCLOSURE
  • This disclosure, in general, relates to elastomer modified perfluoropolymer sheet materials.
  • BACKGROUND
  • Fabric reinforced polytetrafluoroethylene (PTFE) composites are employed in a variety of industries. In general, such composites are known to be resistant to the accumulation of dirt and grime and have a low coefficient of friction. However, conventional reinforced PTFE composites generally have a firm hand and drape. In other words, conventional reinforced PTFE composites are stiff and springy and cannot be formed into compound or double curve shapes without wrinkling or creasing. Furthermore, such conventional composites can have little sound dampening capability and can rattle and pop when deformed.
  • Other conventional solutions have attempted to coat the reinforced PTFE composite with an elastomer. However, such solutions add expense and process complexity. In addition, such solutions are difficult to produce with consistent quality.
  • As such, an improved sheet material would be desirable.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The present disclosure may be better understood, and its numerous features and advantages made apparent to those skilled in the art by referencing the accompanying drawings.
  • FIG. 1, FIG. 2, FIG. 3, and FIG. 4 include illustrations of exemplary sheet materials.
  • FIG. 5 and FIG. 6 include illustrations of exemplary automobile HVAC systems.
  • The use of the same reference symbols in different drawings indicates similar or identical items.
  • DESCRIPTION OF THE DRAWINGS
  • In a particular embodiment, the sheet material includes a blend of a perfluoropolymer and a silicone polymer. The silicone polymer forms about 2 wt % to about 30 wt % of the blend. The sheet material can include additional layers. For example, the sheet material can include a reinforcement layer. The reinforcement layer can include a fibrous material, such as a PTFE coated fiberglass material. In another example, the sheet material is a standalone sheet material without additional layers or reinforcement.
  • In an embodiment, the sheet material can be formed by coating a carrier with a polymer dispersion. The dispersion includes a perfluoropolymer and silicone polymer in an amount of 2% to 30% by weight based on the total weight of the solids in the dispersion. The dispersion can be an aqueous dispersion. Once the carrier is coated with the dispersion, the coating can be dried and sintered or fused. In an example, the carrier includes a reinforcement material that is incorporated into the sheet material upon sintering or fusing of the coating. In another example, the carrier is detachable from the sheet material formed of the coating material, resulting in a sheet material absent reinforcement.
  • In an embodiment, the sheet material is a standalone sheet material absent reinforcement. For example, the sheet material 100 illustrated in FIG. 1 includes a layer 102 formed of a blend of perfluoropolymer and silicone polymer. As illustrated, the material 100 is free of reinforcement. Alternatively, additional layers can be disposed on either major surface of the layer 102.
  • In an example, the blend includes a fluorinated polymer. The fluorinated polymer can be a homopolymer of fluorine-substituted monomers or a copolymer including at least one fluorine-substituted monomer. Exemplary fluorine substituted monomers include tetrafluoroethylene (TFE), vinylidene fluoride (VF2), hexafluoropropylene (HFP), chlorotrifluoroethylene (CTFE), perfluoroethylvinyl ether (PEVE), perfluoromethylvinyl ether (PMVE), and perfluoropropylvinyl ether (PPVE). Examples of fluorinated polymers include polytetrafluoroethylene (PTFE), perfluoroalkylvinyl ether (PFA), fluorinated ethylene-propylene copolymer (FEP), ethylene tetrafluoroethylene copolymer (ETFE), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), and TFE copolymers with VF2 or HFP. In particular, the blend includes a perfluoropolymer, such as PTFE, polyhexafluoropropylene (HFP), fluorinated ethylene propylene (FEP), perfluoroalkylvinyl (PFA), or any combination thereof. In a particular example, the perfluoropolymer includes polytetrafluoroethylene (PTFE). In an embodiment, the perfluoropolymer is derived from a dispersion, such as an aqueous dispersion.
  • The silicone polymer can include a polysiloxane. For example, the silicone polymer can include a polyalkylsiloxane, a phenylsilicone, a fluorosilicone, or any combination thereof. In an example, a polyalkysiloxane includes a polydimethylsiloxane, a polydipropylsiloxane, a polymethylpropylsiloxane, or any combination thereof. In particular, the silicone polymer can be derived from an aqueous dispersion of precured silicone polymers. In an example, the silicone polymer can be derived from an aqueous dispersion and can include precured silicone with terminal end groups that undergo condensation reaction during drying. In particular, the silicone polymer can be derived from an aqueous dispersion of precured silicone with terminal groups or additives, such as cross-linkers, that undergo a condensation reaction when dried. For example, the silicone polymer can be selected from a silicone polymer dispersion available from Wacker-Chemie GmbH, Munchen, Germany, such as the Wacker CT27E silicone rubber dispersion, available from Dow Corning, such as Additive 84, or available from Shin Etsu, such as Polon MF 56.
  • The blend can include silicone polymer in an amount in a range of 2 wt % to 30 wt % based on the total weight of the fused blend. For example, the blend can include silicone polymer in an amount in a range of 5 wt % to 30 wt %, such as a range of 10 wt % to 30 wt %, or even a range of 15 wt % to 20 wt %. In addition, the blend can include fluoropolymer, such as perfluoropolymer, in an amount in a range of 70 wt % to 98 wt %, such as a range of 75 wt % to 90 wt %, or even a range of 80 wt % to 85 wt %.
  • Optionally, the blend can include fillers. For example, the blend can include fillers, light stabilizers, pigments, and bonding aids. Exemplary fillers include talc, silica, and calcium carbonate. Exemplary light absorbing additives and pigments include TiO2, Fe2O3, carbon black, and calcined mixed metal oxides. Such fillers can be included in the blend in an amount not greater than 60 wt %, such as not greater than 40 wt %, not greater than 15 wt %, or even not greater than 5 wt %.
  • In another embodiment, the sheet material can include a reinforcement. For example, as illustrated in FIG. 2, a sheet material 200 includes a reinforcement layer 202. A layer 204 formed of a blend of perfluoropolymer and silicone polymer, such as the blend described above, is disposed on the reinforcement layer 202. For example, layer 204 can contact the reinforcement layer 202 directly without intervening layers, such as adhesive or surface treatment.
  • The reinforcement layer 202 can include a fibrous reinforcement, such as a woven or nonwoven fibrous reinforcement. For example, the fibrous reinforcement can be a woven fabric or an intermeshing of random fibrous strands. In one exemplary embodiment, the fabric is a woven glass fabric. In other embodiments, the reinforcement can include a mesh of ceramic, plastic, or metallic material or sheets of composite materials, among others. Alternatively, the reinforcement layer 202 can take the form of a substrate, typically a sheet. Embodiments can use supports formed of high melting point thermoplastics, such as thermoplastic polyimides, polyether-ether ketones, polyaryl ketones, polyphenylene sulfide, and polyetherimides; thermosetting plastics, particularly of the high temperature capable thermosetting resins, such as polyimides; coated or laminated textiles based on the above thermoplastics or similar thermally stable resins and thermally stable reinforcements such as fiberglass, graphite, and polyaramid; plastic coated metal foil; and metallized or metal foil laminated plastic films. In addition, exemplary embodiments include woven and non-woven materials formed of fibers selected from aramid, fluorinated polymer, fiberglass, graphite, polyimide, polyphenylene sulfide, polyketones, polyesters, or a combination thereof. In particular, the fibrous reinforcement includes a fiberglass reinforcement that has been cleaned or pretreated with heat. Alternatively, the fibrous reinforcement can be a coated fiberglass reinforcement. In a particular example, each of the fibers of the fiberglass can be individually coated with a polymeric coating, such as a fluoropolymer coating, for example, PTFE.
  • The layer 204 can include the blend described above in relation to layer 102 of FIG. 1. The layer 204 can be applied in an amount of at least 1.5 osy. Given that a woven fibrous reinforcement can undulate, the amount of the layer is provided in weight per area (ounces per square yard (osy)). For example, the layer can be applied in an amount of at least 1.8 osy, such as at least 2.0 osy, at least 4.0 osy, at least 4.5 osy, or even at least 6.0 osy. In general, the coating is applied in an amount not greater than 50 osy.
  • In a further embodiment, the blend of perfluoropolymer and silicone elastomer can be applied over a coated reinforcement. For example, as illustrated in FIG. 3, a sheet material 300 can include a reinforcement layer 302 that is coated with layer 304. The layer 304 can be further coated with a layer 306 that includes a blend of perfluoropolymer and silicone polymer, such as the blend described above.
  • The reinforcement layer 302 can be a fibrous woven or nonwoven reinforcement material, as described above in relation to layer 202 of FIG. 2. The fibrous reinforcement can be coated with a layer of perfluoropolymer, such as PTFE, FEP, PFA, or any combination thereof. For example, the layer 304 can be applied in an amount of at least 0.5 osy. For example, the layer 304 can be applied in an amount in a range of 0.5 osy to 2.5 osy, such as 0.5 osy to 2.0 osy, 0.5 osy to 1.5 osy, or 0.5 osy to 1.0 osy.
  • The layer 306 can be applied over and disposed on the layer 304. In particular, the layer 306 can directly contact the layer 304 absent any intervening layers, such as adhesive or surface treatment. The layer 306 includes a blend of perfluoropolymer and silicone polymer, such as the blend described above in relation to layer 102 of FIG. 1. In an example, the layer 306 is applied in an amount of at least 1.5 osy, such as at least 1.8 osy, or even at least 2.0 osy. In a particular example, the layer 306 can be applied in an amount of at least 4.0 osy, such as at least 6.0 osy, but in each case, the amount of layer 306 is not greater than 50 osy.
  • In a further embodiment, a top coat can be applied over the blend. For example, a sheet material 400 illustrated in FIG. 4 can include a structure similar to that described in relation to FIG. 3, including a reinforcement 402 coated with a perfluoropolymer layer 404, which is in turn coated with a polymer blend layer 406.
  • A further layer 408 can be applied over and disposed on the polymer blend layer 406, for example, directly contacting layer 406 without intervening layers. The additional layer 408 can be formed of a perfluoropolymer, such as PTFE, FEP, PFA, or any combination thereof. In particular, the further layer 408 can be applied in an amount in a range of 0.5 osy to 2.5 osy, such as a range of 0.5 osy to 2.0 osy, a range of 0.5 osy to 1.5 osy, or a range of 0.5 osy to 1.0 osy.
  • Alternatively, the layer 408 can include a hard silicone coating, such as a silicone coating having a durometer of at least about 90 as measured on a Shore A scale, or at least about 20, as measured on a Shore D scale. As a result, the layer 408 provides the surface of the sheet material 400 with desired non-tack and low friction properties. For example, the layer 408 can have hardness at least about 95, such as at least about 100 on the Shore A scale. In general, the layer 408 is relatively harder than the layer 406. Further, hardness can be modified by, for example, modification of cross-link density, incorporation of fillers, or any combination thereof.
  • Furthermore, one or more additional layers can be provided which can impart surface functionality to the sheet material. While each of the above embodiments illustrated in FIGS. 2-4 are symmetric about the reinforcement layers, the layers can alternatively be applied in an asymmetric form, wherein one or more of the layers can be absent from one of the sides or each of the layers can be applied in different thicknesses on different sides. The layers can be applied as fused layer or semifused layers. Semifused layers can be adhered to semifused layers of other films, substrates, fabrics, or sheets, and fused to bond the sheet material to the other material.
  • In an example, the total weight of the coated fabric can be at least 4.0 osy. For example, the total weight of the coated fabric can be at least 4.5 osy, such as at least 6.0 osy, or even at least 10 osy. In addition, the fabric can have a total thickness of at least 3.5 mils, such as at least 5.0 mils, or even at least 9 mils. In general, the fabric has a total weight of not greater than 60 osy and a thickness not greater than 100 mils.
  • In particular, the sheet material exhibits a desirable stiffness and hand which remarkably exhibits near isotropy with respect to the machine direction and the cross direction. For example, the sheet material can exhibit a Gurley stiffness in the machine direction of not greater than 550. In particular, the Gurley stiffness in the machine direction is not greater than 525, such as not greater than 500. In the cross direction, the Gurley stiffness is not greater than 800, such as not greater than 600, or even not greater than 500. More particularly, the coated fabric can have a Gurley Directional Ratio, defined as the ratio of the Gurley stiffness in the cross direction over the Gurley stiffness in the machine direction, of not greater than 1.3. For example, the Gurley Directional Ratio can be not greater than 1.1, such as not greater than 1.0.
  • Further, the sheet material exhibits desirable trapezoidal tear strength in both the machine direction and the cross direction. As with the Gurley stiffness, the trapezoidal tear strength in both the machine and cross directions is more closely matched. For example, the trapezoidal tear strength in the machine direction can be at least 13 lbs, such as at least 16 lbs, at least 22 lbs, or even at least 25 lbs. In a further example, the trapezoidal tear strength of the sheet material can be at least 11 lbs in the cross direction, such as at least 13 lbs, at least 16 lbs, or even at least 20 lbs. Trapezoidal tear strength is measured in accordance with ASTM D751 as modified by D4969. The Tear Directional Ratio, defined as the ratio of the trapezoidal tear strength in the cross direction over the trapezoidal tear strength in the machine direction is at least 0.77. For example, the Tear Directional Ratio can be at least 0.81, such as at least 0.85.
  • While the value of Gurley stiffness and trapezoidal tear strength can be influenced by the selection of a reinforcement layer, the sheet material exhibits an unexpected and desirable change in Gurley stiffness or trapezoidal tear strength relative to fabrics of similar weight formed from similar reinforcement and PTFE alone. For example, the Gurley stiffness can be at least 10% less than a PTFE coated fabric, such as at least 18% less, at least 25% less, or even at least 30% less. The percent decrease in Gurley stiffness relative to the reinforcement coated with PTFE alone is defined as the Gurley Index. Further, the trapezoidal tear strength can be at least 25% more than a PTFE coated fabric, such as at least 50% more, at least 70% more, or even at least 90% more. The increase in trapezoidal tear strength relative to the reinforcement coated with PTFE alone is defined as the Tear Index.
  • Further, the sheet material can exhibit a specular reflectance of not greater than 0.5%, such as not greater than 0.2%, as measured in accordance with ASTM E424. In addition, the surface can have a coefficient to friction of not greater than 0.2.
  • The sheet material can provide a cohesive structure that has a desirable coating adhesion as determined by ASTM D4851-88 modified by heating and pressing for as much as 2 minutes to form test samples and performing tests on samples 1″ in width. For example, the coating adhesion can be at least 1.8 lbs/in, such as at least 2.0 lb/in, at least 2.5 lb/in, at least 3.0 lb/in, at least 3.5 lb/in, at least 4.0 lb/in, or even at least 4.5 lb/in.
  • In another example, the sheet material can have a warp break strength (break strength in the machine direction) of at least 270 lb/in, such as at least 290 lb/in, at least 300 lb/in, or even at least 350 lb/in. In addition, the sheet material exhibits a desirable fill break strength (break strength in the cross direction) of at least 200 lb/in, such as at least 230 lb/in, at least 250 lb/in, or even at least 270 lb/in. Strength is determined in accordance with ASTM D3751.
  • Advantageously, the sheet material exhibits improved break strength in the warp or machine direction relative to a comparable sheet material formed of a similar reinforcement and coated with an equivalent thickness of perfluoropolymer, such as PTFE. The Warp Strength Index, defined as the percent increase in warp break strength relative to the comparable sheet material, is at least 8%, such as at least 10%, at least 12%, or even at least 15%.
  • Further, the sheet material exhibits desirable retention of break strength when stressed through creasing or folding. Based on the Flex Fold test according to ASTM D3751 using a 10 lb roller, the sheet material retains a percentage of its warp break strength. The sheet material can exhibits a Strength Retention, defined as the warp break strength retained by a sample after undergoing a Flex Fold test expressed as a percentage of the original warp break strength prior to flexing, of at least 25%, such as at least 35%, or even at least 40%.
  • In an additional example, the sheet material also exhibits a desirable combination of cohesion and break strength. In contrast to other materials that exhibit a trade-off between cohesiveness (measured as coating adhesion) and break strength, the sheet material can exhibit both improved break strength and coating adhesion. As such, the sheet material can exhibit a Cohesive Ratio, defined as the warp break strength divided by the coating adhesion, of not greater than 142.5, such as not greater than 100, not greater than 85, or even not greater than 75.
  • In a further example, the sheet material exhibits low permeability. In particular, the sheet material is not porous or layers that may be porous, such as a layer comprising the perfluoropolymer/silicone blend, include pores that are not substantially interconnected or are localized to that layer. For example, the sheet material can have a permeability of not greater than 0.001 cuin/min, as measured in accordance with ASTM D737, such as having a permeability of approximately 0 cuin/min within the sensitivity of the measuring device. As such, the sheet material can be impermeable. In a particular example, a sheet material including a reinforcement layer and a layer comprising the fluoropolymer/silicone blend described above has a permeability of not greater than 0.001 cuin/min.
  • In an additional example, the sheet material exhibits low permeability when exposed to hydrocarbons and solvent. For example the vapor transmission rate (VTR) permeation when measured in accordance with ASTM D814 under exposure to Fuel B, is not greater than 2.0 mg/s*m2, such as not greater than 1.5 mg/s*m2, not greater than 1.0 mg/s*m2, not greater than 0.5 mg/s*m2, or even not greater than 0.3 mg/s*m2.
  • To form the sheet material, a dispersion can be prepared including a blend of perfluoropolymer particles and precured silicone elastomer particles. For example, the dispersion can be an aqueous dispersion. In a particular example, a dispersion of perfluoropolymer, such as PTFE, is mixed with a dispersion of precured silicone polymer. The silicone polymer can form between 2 wt % and 30 wt % based on the solids of the dispersion. For example, the silicone polymer can form 5 wt % to 30 wt % of the solids of the dispersions, such as 10 wt % to 30 wt %, 10 wt % to 25 wt %, or even 15 wt % to 20 wt % of the solids of the dispersion. The perfluoropolymer can form the remainder of the solids of the dispersion. For example, the perfluoropolymer can form 70 wt % to 98 wt % of the solid content of the dispersion, such as 75 wt % to 90 wt % or even 80 wt % to 85 wt % of the solid content of the dispersion. Alternatively, a solid filler can be included in the dispersion. For example, the solid filler can form not greater than 60 wt % of the solids in the dispersion, such as not greater than 40 wt %, not greater than 15 wt %, or not greater than 5 wt %.
  • A carrier can be coated with the dispersion through a process, such as dip coating, knife coating, or casting. Excess material can be wiped and the coating dried and sintered or fused. For example, the carrier can be a solid material that can be separable from the sheet material. In such a case, the sheet material including a layer of the blend can be formed by first coating the carrier, drying and sintering the material, and separating the material from the carrier to form a sheet material. In such an example, the sheet material is free of a reinforcement layer.
  • In an alternative embodiment, the carrier can be a reinforcement material, which can be coated with the dispersion. The reinforcement material can be a fibrous reinforcement and in particular, can be a coated fibrous reinforcement. In a particular embodiment, the fibrous reinforcement, such as a fiberglass, can be drawn through an aqueous dispersion. To form an optional coating prior to coating with the blend, the aqueous dispersion can be a dispersion of perfluoropolymer absent the silicone. For example, the reinforcement material can be drawn through an aqueous dispersion of PTFE. The fibrous reinforcement coated with the aqueous dispersion is passed through a wiping arrangement to remove excess perfluoropolymer dispersion and is passed through an oven. The oven can be, for example, a three zone tower oven. In particular, the three zone tower oven can fuse the coated material. For example, the first zone can dry the dispersion at a temperature in a range of 200° F. to 300° F. The second zone can heat the deposited perfluoropolymer to remove surfactants and other additives. In particular, the second zone can heat the deposited perfluoropolymer at a temperature in a range of 500° F. to 600° F. The third zone can melt, sinter, or fuse the perfluoropolymer. For example, the third zone can fuse the perfluoropolymer at a temperature in the range of 680° F. to 700° F.
  • In another example, the three zone tower can be set to semifuse the coated material. For example, the first zone can dry the dispersion at a temperature in a range of 200° F. to 300° F. The second zone can heat the deposited perfluoropolymer to remove surfactants and other additives. In particular, the second zone can heat the deposited perfluoropolymer at a temperature in a range of 500° F. to 600° F. The third zone can be set to a temperature lower than the melting point of the perfluoropolymer. For example, the third zone can be set to a temperature in the range of 550° F. to 600° F.
  • To deposit the blended dispersion that includes perfluoropolymer and silicone elastomer, the process can be repeated. For example, the fibrous reinforcement, such as an uncoated fibrous reinforcement or the coated fibrous reinforcement, can be drawn through a bath of aqueous dispersion including the blend of perfluoropolymer and silicone elastomer. Excess dispersion can be removed using a wiping arrangement, such as a metering bar, a Bird bar, a wire-wound metering bar, a K bar, or other similar equipment or combinations thereof. The reinforcement material coated with the blended dispersion is heated. For example, the dispersion can be heated to dry the dispersion, remove surfactants or other additives and subsequently to melt the perfluoropolymer and cure the precured silicone polymer. In particular, the coated reinforcement material can pass through a three zone tower oven, including a first zone that dries the dispersion at a temperature in a range of 200° F. to 300° F. A second zone of the oven can remove surfactants and other additives from the deposited blend coating at a temperature in a range of 500° F. to 600° F. The third zone can be set to fuse the blend, for example, melt the perfluoropolymer, or can be set to form a semifused layer. For example, the third zone can be set to a temperature in a range of 680° F. to 700° F. to fuse the material. In another example, the third zone can be set to a temperature in a range of 550° F. to 600° F. to semifuse the layer. Alternatively, the coating can be heating in an oven including one zone, two zones, or more. In a particular example, the coating can be dried and sintered in two stages.
  • In addition, particularly when the outer layer is a semifuse layer, the sheet material can be pressed or calendered. In an example, the drums of the calender can be set to a temperature in a range of 275° F. to 400° F. and to a pressure between the drums in a range of 500 psi to 4000 psi. Subsequently, the calendered sheet material including the semifused layer or layers can be subjected to fusing conditions, such as a temperature within a range of 680° F. to 700° F.
  • Further, the sheet material can pass through a cooling plenum from which it can be directed to a subsequent dip pan to begin formation of a further layer of film, to a stripping apparatus, or to a roll for storage. In another embodiment, sheets of composite material are formed and subsequently layered over the reinforcement material. These sheets can be further processed to bond to the reinforcement material. For example, sheets of material can be laminated to the reinforcement material.
  • In a particular example, a reinforcement material can be passed through an emulsion of perfluoropolymer, such as PTFE, and fused. For example, the reinforcement material can be passed through the emulsion once. In another example, the reinforcement material can be passed through a second time, or optionally a third time, and fused. Each pass results in additional thickness referred to herein as a pass. Following the application of the perfluoropolymer layer, the sheet material can be passed through an emulsion including a blend of perfluoropolymer and silicone. The sheet material can be passed through the emulsion of the blend at least once. In particular, the sheet material can be passed through the emulsion of the blend twice or can be passed through the emulsion three or more times. Following coating of the blend over the sheet material, the blend layer can be fused. Alternatively, the blend layer can be semifused, as described above, and can be calendered, pressed, or further treated, and subsequently fused.
  • Optionally additional layers can be applied. For example, an additional layer or layers can be coated on the sheet material by passing the sheet material through an additional emulsion. In an example, the additional emulsion can be a perfluoropolymer emulsion. In another example, the additional emulsion can be a silicone emulsion. Passes underlying the additional layers can be fused or semifused when the additional layer is coated. The additional layer or layers can be fused, or can be semifused. The additional layer or layers can be calendered or otherwise treated.
  • In a particular example, a semifused layer, either the blend layer or an additional layer can be pressed into contact with another semifused layer of another sheet material or film. In an example, the construct can be fused to bond the sheet materials or sheet material and film together. For example, an additional semifused PTFE outer layer can be pressed or calendered into contact with a semifused PTFE layer of a second sheet material or film and subsequently fused. In another example, a semifused blend layer can be placed in contact with a semifused blend layer or semifused perfluoropolymer layer of a second sheet material or film, and subsequently fused.
  • In a particular embodiment, the sheet material includes a reinforcement material coated with a single pass of perfluoropolymer, such as PTFE, that is coated with at least one pass and likely two passes of a blend. Each of the layers can be fused. Alternatively, the passes of the blend can be semifused, calendered, and subsequently, fused. In another embodiment, the sheet material includes the reinforcement material, a pass of fused perfluoropolymer, two passes of fused blend, and an outer layer formed of at least one pass of a polymer, such as a perfluoropolymer or a silicone polymer. In an example, the outer layer is fused. In another example, the outer layer is semifused.
  • In a further embodiment, an outer layer that is semifused or a blend layer that is semifused can be placed in contact with a film, such as a film including perfluoropolymer or silicone. In an example, the film is a defect free perfluoropolymer film, such as a PTFE film. In an example, a film has a more uniform consistency than a coating and lower variability in properties. An example of a film includes a skived film, a cast film, or an extruded film.
  • Remarkably, it has been discovered that the dispersion including the blend of perfluoropolymer and silicone polymer permits thicker coatings to be applied in a single pass. For example, in a single pass, a dispersion of the blend can be coated to form a coating having a weight of at least 1.5 osy, such as at least 1.8 osy, at least 2.0 osy, or even at least 2.4 osy. Generally, coatings of PTFE when coated to form layers of weight greater than 1.0 osy form cracks, deformations or surface irregularities unless the coating is performed in multiple passes.
  • The coated fabric formed through such a process and as described above in relation to the FIGS. 1-4 is particularly well suited for use in automobile HVAC film valves. For example, as illustrated in FIG. 5 and FIG. 6, a sheet material 502 formed as described above can be particularly well suited as a film valve. For example, in the automobile HVAC system 500 illustrated in FIG. 5, the film valve can extend between rollers 504. A film valve 502 can be drawn between rollers 504 to align holes 608, 610, and 612 as illustrated at FIG. 6 with vents 508. Depending on the alignment of the holes 608, 610, and 612 with the vents 508, a source of air, such as a fan, can direct air through the film valve 502 and into one or more of the vents 508.
  • Advantageously, embodiments of the sheet material described above exhibit desirable flexibility and hand as well as other desirable features which make the sheet material particularly well suited for use in automobile HVAC systems. In addition, embodiments of the sheet material have greater sound absorption than a PTFE coated fabric having the same reinforcement.
  • In a particular example, the sheet material exhibits desirable properties, including breaking strength and crease and tear strength resistance, as well as, conformability, which enhance the useful life of the material. As such, the sheet material is particularly suited for use as a high temperature release sheet or as a belt in industrial applications.
  • For example, in photovoltaic lamination, the release fabric (whether in sheet or belt form) is forced to conform somewhat to the irregular contours of the photovoltaic cell through vacuum or mechanical pressure. Such forced conformation can cause the photovoltaic material to distort, which can cause creases that lead to defects in the photovoltaic cells being produced. Additionally, the conventional material can be severely weakened after repeated pressing cycles and can fail to due breaking or tearing. The present sheet material withstands repeated press cycles until loss of release properties, and not from mechanical failure. The enhanced physical properties allow the release fabric to remain in place longer, reducing the number of change outs due to premature failure.
  • In addition, release applications rely on the physical properties of the reinforcing material as much as the non-stick property of the perfluoropolymer. Such applications include other laminating or pressing operations in textiles, automotive and general industrial applications. Sealing of plastic packaging, whether rigid shapes like battery packages or thin flexible films that encase toilet paper and paper towels benefit from the high improved tensile strength, higher crease and tear resistance strength as well as the improved conformability of the present sheet material, as the release sheets and belting products through which heat is applied to form or seal these materials conform to irregular shapes and materials of various hardness (i.e., the core in the toilet paper or paper towel relative to the toilet paper itself). Additionally, adhesive backed pressure sensitive tape products are used in similar applications, and often conform to irregular heat sealing jaws, wires or molds. In contrast to conventional sheet materials, the present sheet material is useful in applications where the release fabric or tape is not kept in a planar shape. In such applications, the present sheet material exhibits increased useful release life.
  • In a further example, the present sheet material can be useful in insulator jacketing, bladder applications, expansion joints, HVAC control films, photovoltaic release sheets, and floating roof seals. Embodiments including food grade silicone can also be used in the food and food services industries, for example, as spill mats or industrial cooking belts, among other food preparation apparatuses.
  • EXAMPLES Example 1
  • A sample of industry-style 1080 fiberglass fabric, greige finish, weighing 1.38 ounces per square yard (osy) after heat cleaning, with thickness of 2.1 mils, is lightly coated with fused PTFE resin by drawing the fabric through a bath of PTFE aqueous dispersion, DuPont TE-3859, reduced with water to 1.25 specific gravity. The coated fabric is passed through a wiping arrangement to remove excess PTFE dispersion and is passed through a three-zone tower oven, which in the first zone dries the dispersion at a temperature in a range of 200° F. to 300° F., in the second zone heats the deposited PTFE resin at a temperature in a range of 500° F. to 600° F., and in the third zone melts the PTFE at a temperature in a range of 680° F. to 700° F. The coated fabric weighs about 2.02 osy.
  • A second coating from a dispersion mixture of the DuPont TE-3859 PTFE dispersion and a silicone rubber dispersion, Wacker Silicones Finish CT27E (Wacker Silicones, Adrian, Mich.) is coated on to the coated fabric by drawing the coated fabric through the dispersion and wiping excess dispersion from the coated fabric. The dispersion mixture is made by combining by simple stirring about 131 parts by weight (pbw) of the DuPont TE-3859 with about 31 pbw of the Wacker CT27E. The mixture is not reduced with water.
  • The coating, comprising about 80 weight percent of PTFE and 20 weight percent of silicone rubber, is applied using the process described above, except that the wiping arrangement was modified to allow a greater weight of the coating formulation to be applied. The subsequent total weight of the coated fabric is 4.24 osy and is 0.0035 inches thick.
  • A second sample is prepared using a similar, two-step process, with an industry style 2116 fiberglass fabric, greige finish, weighing after heat cleaning 3.13 osy, with 3.7 mils thick. The intermediate PTFE-coated fabric weighs about 3.79 osy and the finished product weighs about 6.24 osy. The finished product is about 0.0052 inches thick.
  • The two samples are measured for finished thickness, finished weight, and coefficient of friction. In addition, the two samples are tested for break strength, load, trapezoidal tear strength, and coating adhesion, as illustrated in Table 1.
  • TABLE 1
    Properties of Coated Fabric
    Property/attribute Units Sample 1 Sample 2
    Finished thickness mil 3.5 5.2
    Finished weight osy 4.2 6.2
    Breaking strength, warp lbf/in 110 130
    Load at 2% elongation, lbf/in 65 63
    warp
    Trap tear, fill lbf 4.2 4.7
    Coefficient of friction 0.16 0.16
    Coating adhesion lb/in 3.3 2.1
  • Example 2
  • An additional sample is prepared using the method described in Example 1. The base fabric is an industrial style 7628 fiberglass fabric having a standard weight of 5.94 osy after cleaning. An initial coating of PTFE is applied as described in relation to Example 1. The blend coating composition described above is applied in three passes. The weight of the fabric prior to application of the blend coating is 7.3 osy and following each of the three passes is 9.06 osy, 11.57 osy, and 12.39 osy, respectively. The final thickness of the film is 0.0103 in.
  • The sample (Sample 3) is compared to a standard 10 mil PTFE film (PTFE CF210) based on the same base fabric. The sample and comparative sample are tested for Gurley stiffness, trapezoidal tear strength (ASTM D751), and specular reflectance (ASTM E424).
  • TABLE 2
    Comparative Testing of Samples
    PTFE CF210 Sample 3 % Change
    Gurley Stiffness Mach. Dir. 607 490 −19.2
    Gurley Stiffness Cross Dir. 940 477 −49.2
    Trap. Tear Mach. Dir. (lbs) 14.7 25.7 74.8
    Trap Tear Cross Dir. (lbs) 10.8 22.5 100.8
    Specular Reflectance (%) 0.99 0.05 −94.9
  • In addition to exhibiting lower Gurley stiffness in both directions relative to the comparative sample, the blend sample exhibits a lower difference between stiffness in machine versus cross directions. In particular, the Gurley Directional Ratio is less than 1.0, i.e., 0.97, whereas the comparative sample exhibits a Gurley Directional Ratio significantly greater than 1.0. Similarly, the tear strength of the sample is higher than that of the comparative sample and the ratio between the directions is closer to 1. The specular reflectance of the blend sample is lower. Additional coatings can be used to manipulate the reflectance.
  • While the value of the Gurley stiffness and the trapezoidal tear strength can be influenced by the 7628 fiberglass fabric, the change relative to the PTFE coated fabric and the directional ratios represent an unexpected and desirable improvement.
  • Example 3
  • Samples and comparative samples are prepared using an industrial standard 1528 fiberglass fabric. The samples are coated in passes that are fused. The samples and comparative samples are tested for mechanical properties, including machine direction trapezoidal tear strength, cross direction trapezoidal tear strength, warp (machine direction) break strength, fill (cross direction) break strength, strength retention, and coating adhesion.
  • Comparative samples (Comparative Samples 1 and 2) are prepared by repeated passes of the 1528 fiberglass fabric through a PTFE emulsion to form a sheet material having a weight of 13.5 osy. The PTFE coating is fused.
  • A first sample (Sample 4) is prepared by applying a single fused pass of clear PTFE to the 1528 fiberglass fabric, followed by two semifused passes of a blend of PTFE and 20 wt % silicone, formed as describe in relation to Example 1. After application of the semifused passes, the blend layer is fused. A single pass of fused PTFE is applied over the blend layer.
  • A second sample (Sample 5) includes the 1528 fiberglass fabric and a pass of fused clear PTFE, coated with three passes of semifused blend including 10% silicone. The semifused passes are fused to form a blend layer that is subsequently coated with a fused clear PTFE layer.
  • A third sample (Sample 6) includes the 1528 fiberglass fabric and two passes of fused clear PTFE, coated with two passes of semifused blend including 20% silicone. The semifused passes are calendered and fused to form a blend layer that is subsequently coated with a fused clear PTFE layer.
  • A fourth sample (Sample 7) includes the 1528 fiberglass fabric and two passes of fused clear PTFE, coated with two passes of semifused blend including 20% silicone. The semifused passes are calendered and fused to form a blend layer that is subsequently coated with a fused clear PTFE layer. The sample is further subjected to an additional calendering.
  • A fifth sample (Sample 8) includes the 1528 fiberglass fabric and a single pass of fused clear PTFE, coated with two passes of semifused blend including 20% silicone. The semifused passes are coated with a semifused clear PTFE layer. The material is subjected to calendering, followed by fusing. An additional clear PTFE pass is fused to the material.
  • Table 3 illustrates the weight and mechanical properties of the samples and comparative samples. As illustrated, the samples exhibit desirable improvement in break strength. In addition, the samples exhibit a desirable Cohesion Ratio and Strength Retention.
  • TABLE 3
    Properties of Samples including 1528 Fiberglass Fabric
    Property C1 C2 4 5 6 7 8
    Weight osy 13.5 13.5 13.9 13.0 13.7 13.7 14.6
    Thickness mil 10 10 10 9.8 10 10 10
    Warp Trap Tear lb 14.9 13.0 16.3 14.2 14.7 13.7 13.7
    Fill Trap Tear lb 13.8 13.7 16.3 11.5 12.8 12.9 11.4
    Warp Break Strength lb/in 262 243 294.6 294.7 300.7 290.7 277.8
    Strength Retention % N/A N/A 36.8 40.9 41.5 34.0 26.2
    Coating Adhesion lb/in 1.7 1.7 3.68 4.77 4.84 4.67 3.83
    Cohesion Ratio 154 143 80 62 62 62 72
  • Example 4
  • Samples and comparative samples are prepared using an industrial standard 7628 fiberglass fabric. The samples are coated in passes that are fused. The samples and comparative samples are tested for mechanical properties, including machine direction trapezoidal tear strength, cross direction trapezoidal tear strength, warp (machine direction) break strength, fill (cross direction) break strength, strength retention, and coating adhesion.
  • Comparative samples (Comparative Samples 3 and 4) are prepared by repeated passes of the 7628 fiberglass fabric through a PTFE emulsion to form a sheet material having a weight of 12.7 osy. The PTFE coating is fused.
  • A first sample (Sample 9) is prepared by applying two pass of clear PTFE that are fused to the 7628 fiberglass fabric, followed by three semifused passes of a blend of PTFE and 20 wt % silicone. After application of the semifused passes, the blend layer is fused. A single pass of fused PTFE is applied over the blend layer.
  • A second sample (Sample 10) includes the 7628 fiberglass fabric and a pass of fused clear PTFE, coated with two passes of semifused blend including 20 wt % silicone. The semifused passes coated with a semifused clear PTFE layer and calendered. The calendered sheet material is fused, followed the application of a fused clear PTFE pass.
  • Table 4 illustrates the weight and mechanical properties of the samples and comparative samples. As illustrated, the samples exhibit a desirable break strength and desirable Strength Retention and Cohesion Ratio.
  • TABLE 4
    Properties of Sheet Materials having 7268 Fiberglass Fabric
    Property C3 C4 9 10
    Weight osy 12.7 12.7 13.9 13.6
    Thickness mil 9.7 9.7 10 10
    Warp Trap Tear lb 26.0 26.4 25.8 21.2
    Fill Trap Tear lb 21.0 21.4 21.7 21.1
    Warp Break Strength lb/in 347 421 424 360
    Strength Retention % N/A N/A 42.2 38.0
    Coating Adhesion lb/in 3.0 3.0 2.98 2.53
    Cohesion Ratio 115 140 143 142
  • Example 5
  • Samples are prepared using a 7628 fiberglass fabric or a 1564 fiberglass fabric. To the fiberglass fabric, a clear PTFE coating is applied and fused, followed by a single pass coating of a blend including 20 wt % silicone and PTFE, which is semifused. A 1 mil PTFE film is laminated to the semifused blend layer and the construction is fused.
  • Example 6
  • Samples are prepared using a 7628 fiberglass fabric or a 1528 fiberglass fabric. To the fiberglass fabric, a clear PTFE coating is applied and fused, followed by two pass coating of a blend either including 5 wt % or 10 wt % silicone and PTFE, which is subsequently fused. A pass of clear PTFE is applied on the blend layer and fused.
  • Example 7
  • Samples are formed in accordance with Example 5. Sample 11 includes a 7628 greige fiberglass fabric, and Sample 12 includes a 1564 greige fiberglass fabric. Properties of the samples are compared with those of CPI-10 42.5″ (C5) and CPI-18 42.5″ (C6), both available from Saint-Gobain. Table 5 illustrates the properties.
  • TABLE 5
    Properties of Laminated Samples
    Sample 11 C5 Sample 12 C6
    Before After PQD Before After PQD
    Weight oz/sq yd 13.68 13.78 14.5 23.99 24.31 22.5
    Thickness mils 10.7 10.7 10.5 21.0 20.5 19.0
    Ultimate Tensile (W) PLI 352 361 325 531 524 N/A
    Elongation (W) % 6 6 N/A 6 6 N/A
    Ultimate Tensile (F) PLI 265 253 225 494 506 N/A
    Elogation (F) % 5 5 N/A 10 10 N/A
    Trap Tear (W) Lbs 26.9 27.3 23 56.1 55.2 40
    Trap Tear (F) Lbs 28.7 25.6 23 59.0 59.8 50
    VTR (Fuel B) mg/s*m2 <1.0 <1.0 <1.0 <0.3 <0.3 <0.3
    Permeation/ASTM D814
    Temperature (Top Range) ° F. 450 450 500 450 450 500
    W—Warp, F—Fill
  • As is illustrated in Table 5, Samples 11 and 12 exhibit low permeation when exposed to Fuel B. In addition, Samples 11 and 12 exhibit desirable mechanical properties relative to the comparative samples.
  • In a particular embodiment, a coated fabric includes a reinforcement, a first coating disposed on the reinforcement, and a second coating disposed on the first coating. The first coating includes perfluoropolymer. The second coating includes perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %. In an example, the range of silicone polymer is 10 wt % to 25 wt %, such as 15 wt % to 20 wt %.
  • In an example, the coated fabric can include a third coating on the second coating. The third coating can include a fluoropolymer, such as a perfluoropolymer. In another example, the third coating can include silicone.
  • In a further example, the coated fabric has a Gurley stiffness in the machine direction of not greater than 550, such as not greater than 525, or not greater than 500. In an additional example, the coated fabric has a Gurley stiffness in the cross direction of not greater than 800, such as not greater than 600, or not greater than 500. In addition, the coated fabric can have a Gurley Directional Ratio of not greater than 1.3, such as not greater than 1.1, or not greater than 1.0.
  • In a further example, the coated fabric has a trapezoidal tear strength in the machine direction of at least 13 lbs, such as at least 16 lbs, at least 20 lbs, at least 22 lbs, or at least 25 lbs. In another example, the coated fabric has a trapezoidal tear strength in the cross direction of at least 11 lbs, such as at least 13 lbs, at least 16 lbs, or at least 20 lbs. In addition, the coated fabric can have a Tear Directional Ratio of at least 0.77, such as at least 0.81, or at least 0.85. Further, the coated fabric can exhibit a Tear Index of at least 25%.
  • In an additional example, the coated fabric has a specular reflectance of not greater than 0.5%, such as not greater than 0.2%. Further, the coated fabric can have a coefficient of friction of not greater than 0.2. In addition, the coated fabric can have a coating adhesion of at least 1.8 lb/in, such as at least 2.0 lb/in, or at least 2.5 lb/in.
  • In another example, the coated fabric can have a warp break strength of at least 270 lb/in, such as at least 290 lb/in. Further, the fill break strength can be at least 200 lb/in. The coated fabric can exhibit a Strength Retention of at least 25%, such as at least 35%. In addition, the coated fabric can exhibit a Cohesion Ratio of not greater than 142.5, such as not greater than 100.
  • In an example, the perfluoropolymer includes PTFE, HFP, FEP, PFA, or a combination thereof. In a particular example, the perfluoropolymer includes polytetrafluoroethylene. In a further example, the silicone polymer is derived from a precured silicone polymer dispersion, such as a condensation polymerized silicone.
  • In a particular example, the first coating is applied in an amount of at least 0.5 osy. In another example, the second coating is applied in an amount of at least 1.5 osy, such as at least 1.8 osy, at least 2.0 osy, or at least 2.4 osy. The total weight of the coated fabric can be at least 4.0 osy, such as at least 4.5 osy, or at least 6.0 osy.
  • In another embodiment, a sheet material includes a blend of perfluoropolymer and silicone polymer. The blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %. The sheet material has a Gurley Directional Ratio of not greater than 1.3.
  • In a further embodiment, a sheet material includes a blend of perfluoropolymer and silicone polymer. The blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %. The sheet material has a Tear Directional Ratio of at least 0.77.
  • In an additional embodiment, a sheet material includes a blend of perfluoropolymer and silicone polymer. The blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %. The sheet material has a total thickness of at least 9 mils and a Gurley stiffness of not greater than 550.
  • In another embodiment, a venting system includes a plurality of conduits, each having an opening, and includes a film having a plurality of openings. The film is movable to align at least one opening with an opening of at least one of the conduit of the plurality of conduits. The film includes a blend of perfluoropolymer and silicone polymer. The blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • In a further embodiment, a method of forming a sheet material includes coating a reinforcement with a first coating comprising a perfluoropolymer to form a first intermediate article, coating the first intermediate article with a second coating comprising a polymer dispersion to form a second intermediate article, and sintering the second intermediate article. The polymer dispersion includes a perfluoropolymer and a silicone polymer. The dispersion includes the silicone polymer in an amount in a range of 2 wt % to 30 wt % based on the total weight of solids in the polymer dispersion.
  • In an example, coating the first intermediate article with the second coating includes coating the first intermediate article with at least 2.0 osy of the second coating in a single step. In a further example, coating the first intermediate article with the second coating includes coating the first intermediate article with at least 2.4 osy of the second coating in a single step.
  • In an additional embodiment, a method of forming a sheet material includes coating a carrier with at least 2.0 osy of a polymer dispersion comprising a perfluoropolymer and a silicone polymer. The silicone polymer forms 2 wt % to 30 wt % of the solids content of the dispersion. The method further includes drying the polymer dispersion and sintering the dried polymer dispersion.
  • In an example, the carrier forms a carrier web reinforcement that is incorporated into the sheet material. In a further example, the carrier comprises a fibrous reinforcement material. In an additional example, the carrier includes a fibrous reinforcement material coated with a perfluoropolymer. In another example, the carrier is a support separable from the coating and the method further includes delaminating the coating from the carrier.
  • In a further embodiment, a sheet material includes a polymer blend comprising perfluoropolymer and silicone polymer. The polymer blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %. In an example, the sheet material further includes a reinforcement layer, the polymer blend disposed on the reinforcement layer. In an additional example, the reinforcement layer comprises a fibrous reinforcement material. Further, the reinforcement layer can include a fibrous reinforcement material coated with a perfluoropolymer.
  • In a further embodiment, a coated fabric includes a reinforcement material; and a coating overlying the reinforcement material. The coating includes perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %. The coated fabric has a permeability of not greater than 0.001 cuin/min. In an example, the coated fabric is substantially impermeable.
  • In an example, the range of silicone polymer is 10 wt % to 25 wt %, such as 15 wt % to 20 wt %. In another example, the coated fabric has a trapezoidal tear strength in the machine direction of at least 13 lbs. In a further example, the coated fabric has a coating adhesion of at least 1.8 lb/in. In an additional example, the coated fabric exhibits a Strength Retention of at least 25%.
  • In a particular example, the perfluoropolymer includes polytetrafluoroethylene (PTFE), hexafluoropropylene (HFP), fluorinated ethylene propylene (FEP), perfluoroalkyl vinyl ether (PFA), a combination thereof. For example, the perfluoropolymer includes polytetrafluoroethylene (PTFE). The silicone polymer can be derived from a precured silicone polymer dispersion. In particular the silicone can be a condensation polymerized silicone.
  • In another embodiment, a sheet material includes a single layer. The single layer includes a polymer blend comprising perfluoropolymer and silicone polymer. The polymer blend includes the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
  • In an additional embodiment, a method of forming a coated fabric includes dispensing a fabric and applying a first emulsion coating to the fabric. The first emulsion includes a perfluoropolymer. The method also includes fusing the first emulsion coating to form a first layer and applying a second emulsion coating on the first emulsion coating. The second emulsion coating includes a blend of perfluoropolymer and silicone polymer in an amount in a range of 2 wt % to 30 wt %. The method further includes fusing the second emulsion coating to form a second layer.
  • In an example, the method further includes semifusing the second emulsion coating following applying the second emulsion coating and prior to fusing the second emulsion coating. In addition, the method can further include calendering the second emulsion coating following semifusing the second emulsion coating. Further, the method can include contacting the second emulsion coating with a perfluoropolymer film following semifusing the second emulsion coating, wherein fusing the second emulsion coating includes fusing the second emulsion coating while in contact with the perfluoropolymer film.
  • In another example, the method further includes applying a third emulsion coating on the second emulsion coating. In an example, the third emulsion coating includes a perfluoropolymer. In another example, the third emulsion coating includes silicone.
  • Further, the method can include semifusing the third emulsion coating, contacting the third emulsion coating with a film, and fusing the third emulsion coating while in contact with the film. The method can also include semifusing the third emulsion coating, calendering the third emulsion coating, and fusing the third emulsion coating. In addition, applying the third emulsion coating can include applying the third emulsion coating to the second emulsion coating while the second emulsion coating is in a semifused state.
  • As used herein, the terms “over” or “overlie,” when used in relation to location indicate a location relatively closer to an outer surface of the sheet material when moving away from reinforcement material, if any.
  • Note that not all of the activities described above in the general description or the examples are required, that a portion of a specific activity may not be required, and that one or more further activities may be performed in addition to those described. Still further, the order in which activities are listed are not necessarily the order in which they are performed.
  • In the foregoing specification, the concepts have been described with reference to specific embodiments. However, one of ordinary skill in the art appreciates that various modifications and changes can be made without departing from the scope of the invention as set forth in the claims below. Accordingly, the specification and figures are to be regarded in an illustrative rather than a restrictive sense, and all such modifications are intended to be included within the scope of invention.
  • As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having” or any other variation thereof, are intended to cover a non-exclusive inclusion. For example, a process, method, article, or apparatus that comprises a list of features is not necessarily limited only to those features but may include other features not expressly listed or inherent to such process, method, article, or apparatus. Further, unless expressly stated to the contrary, “or” refers to an inclusive-or and not to an exclusive-or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
  • Also, the use of “a” or “an” are employed to describe elements and components described herein. This is done merely for convenience and to give a general sense of the scope of the invention. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.
  • Benefits, other advantages, and solutions to problems have been described above with regard to specific embodiments. However, the benefits, advantages, solutions to problems, and any feature(s) that may cause any benefit, advantage, or solution to occur or become more pronounced are not to be construed as a critical, required, or essential feature of any or all the claims.
  • After reading the specification, skilled artisans will appreciate that certain features are, for clarity, described herein in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features that are, for brevity, described in the context of a single embodiment, may also be provided separately or in any subcombination. Further, references to values stated in ranges include each and every value within that range.

Claims (35)

1. A coated fabric comprising:
a reinforcement;
a first coating on the reinforcement, the first coating comprising perfluoropolymer; and
a second coating on the first coating, the second coating comprising perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %.
2. The coated fabric of claim 1, wherein the range of silicone polymer is 10 wt % to 25 wt %.
3. (canceled)
4. The coated fabric of claim 1, further comprising a third coating on the second coating.
5. The coated fabric of claim 4, wherein the third coating comprises fluoropolymer.
6. (canceled)
7. The coated fabric of claim 4, wherein the third coating comprises silicone.
8. The coated fabric of claim 1, wherein the coated fabric has a trapezoidal tear strength in the machine direction of at least 13 lbs.
9.-11. (canceled)
12. The coated fabric of claim 1, wherein the coated fabric has a trapezoidal tear strength in the cross direction of at least 11 lbs.
13.-14. (canceled)
15. The coated fabric of claim 1, wherein the coated fabric has a Tear Directional Ratio of at least 0.77.
16.-18. (canceled)
19. The coated fabric of claim 1, wherein the coated fabric has a coating adhesion of at least 1.8 lb/in.
20.-23. (canceled)
24. The coated fabric of claim 1, wherein the coated fabric exhibits a fill break strength of at least 200 lb/in.
25. The coated fabric of claim 1, wherein the coated fabric exhibits a Strength Retention of at least 25%.
26. (canceled)
27. The coated fabric of claim 1, wherein the coated fabric exhibits a Cohesion Ratio of not greater than 142.5.
28.-38. (canceled)
39. The coated fabric of claim 1, wherein the coated fabric has a specular reflectance of not greater than 0.5%.
40.-41. (canceled)
42. The coated fabric of claim 1, wherein the perfluoropolymer comprises polytetrafluoroethylene (PTFE), hexafluoropropylene (HFP), fluorinated ethylene propylene (FEP), perfluoroalkyl vinyl ether (PFA), a combination thereof.
43. (canceled)
44. The coated fabric of claim 1, wherein the silicone polymer is derived from a precured silicone polymer dispersion.
45. (canceled)
46. The coated fabric of claim 1, wherein the first coating is applied in an amount of at least 0.5 osy.
47. The coated fabric of claim 1, wherein the second coating is applied in an amount of at least 1.5 osy.
48.-49. (canceled)
50. The coated fabric of claim 1, wherein the total weight of the coated fabric is at least 4.0 osy.
51.-55. (canceled)
56. A coated fabric comprising:
a reinforcement material; and
a coating overlying the reinforcement material, the coating comprising perfluoropolymer and a silicone polymer in an amount in a range of 2 wt % to 30 wt %;
wherein the coated fabric has a permeability of not greater than 0.001 cuin/min.
57.-65. (canceled)
66. A sheet material comprising a single layer, the single layer comprising a polymer blend comprising perfluoropolymer and silicone polymer, the polymer blend comprising the silicone polymer in an amount in a range of 2 wt % to 30 wt %.
67.-88. (canceled)
US12/641,972 2008-12-22 2009-12-18 Modified perfluoropolymer sheet material and methods for making same Expired - Fee Related US8969222B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US12/641,972 US8969222B2 (en) 2008-12-22 2009-12-18 Modified perfluoropolymer sheet material and methods for making same
US14/617,386 US20150299943A1 (en) 2008-12-22 2015-02-09 Modified perfluoropolymer sheet material and methods for making same

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13994608P 2008-12-22 2008-12-22
US24392609P 2009-09-18 2009-09-18
US12/641,972 US8969222B2 (en) 2008-12-22 2009-12-18 Modified perfluoropolymer sheet material and methods for making same

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/617,386 Continuation US20150299943A1 (en) 2008-12-22 2015-02-09 Modified perfluoropolymer sheet material and methods for making same

Publications (2)

Publication Number Publication Date
US20100159223A1 true US20100159223A1 (en) 2010-06-24
US8969222B2 US8969222B2 (en) 2015-03-03

Family

ID=42266558

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/641,972 Expired - Fee Related US8969222B2 (en) 2008-12-22 2009-12-18 Modified perfluoropolymer sheet material and methods for making same
US14/617,386 Abandoned US20150299943A1 (en) 2008-12-22 2015-02-09 Modified perfluoropolymer sheet material and methods for making same

Family Applications After (1)

Application Number Title Priority Date Filing Date
US14/617,386 Abandoned US20150299943A1 (en) 2008-12-22 2015-02-09 Modified perfluoropolymer sheet material and methods for making same

Country Status (9)

Country Link
US (2) US8969222B2 (en)
EP (1) EP2376571B1 (en)
JP (2) JP5612596B2 (en)
CN (1) CN102449061B (en)
CA (2) CA2953354A1 (en)
MX (1) MX2011006681A (en)
RU (1) RU2486216C2 (en)
TW (1) TWI410550B (en)
WO (1) WO2010075210A2 (en)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100044382A1 (en) * 2008-08-22 2010-02-25 Saint-Gobain Performance Plastics Corporation Fluoropolymer coated article
US20110146501A1 (en) * 2009-12-18 2011-06-23 Saint-Gobain Performance Plastics Corporation Cooking release sheet materials and release surfaces
US20130337250A1 (en) * 2012-05-30 2013-12-19 Richard J. Austin Modified perfluoropolymer material
US20140124822A1 (en) * 2012-11-05 2014-05-08 Ledengin, Inc. Graphite-containing substrates for led packages
US20150307670A1 (en) * 2014-04-25 2015-10-29 Saint-Gobain Performance Plastics Corporation Thin low friction liners
US20160097155A1 (en) * 2014-10-07 2016-04-07 Saint-Gobain Performance Plastics Corporation Strength retention fabric
WO2017143097A1 (en) * 2016-02-16 2017-08-24 Saint-Gobain Performance Plastics Corporation Composite and method for making
US20170274694A1 (en) * 2016-03-24 2017-09-28 Saint-Gobain Performance Plastics Corporation Printable fabric
WO2017165384A1 (en) * 2016-03-21 2017-09-28 Saint-Gobain Performance Plastics Corporation Architectural membrane
US10194528B2 (en) * 2011-05-06 2019-01-29 Guangdong Shengyi Sci. Tech Co., Ltd. Composite material, high-frequency circuit baseboard made therefrom and production method thereof
US10626550B2 (en) * 2015-11-24 2020-04-21 Bose Corporation Water-resistant composition
US20200123406A1 (en) * 2016-10-24 2020-04-23 Saint-Gobain Performance Plastics Corporation Polymer compositions, materials, and methods of making
US11174418B2 (en) * 2016-06-27 2021-11-16 William Marsh Rice University Fluorine and hydrogen-based adhesive compositions and methods of making the same
US11326025B2 (en) 2017-02-24 2022-05-10 Lg Chem, Ltd. Polyamideimide copolymer and polyamideimide film comprising the same

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10065339B2 (en) 2013-05-13 2018-09-04 Romeo Ilarian Ciuperca Removable composite insulated concrete form, insulated precast concrete table and method of accelerating concrete curing using same
WO2014186299A1 (en) 2013-05-13 2014-11-20 Ciuperca Romeo Llarian Insulated concrete battery mold, insulated passive concrete curing system, accelerated concrete curing apparatus and method of using same
CA2923717A1 (en) 2013-09-09 2015-03-12 Romeo Ilarian Ciuperca Insulated concrete slip form and method of accelerating concrete curing using same
US20170042371A1 (en) * 2015-02-02 2017-02-16 Jack Lindon Skinner Foldable Food Grade Cooking Surface and Method of Use
TWI774642B (en) * 2015-05-18 2022-08-21 美商阿爾巴尼國際公司 Use of silicone content and fluoropolymer additives to improve properties of polymeric compositions
PL3359597T3 (en) 2015-10-05 2020-07-27 Albany International Corp. Compositions and methods for improved abrasion resistance of polymeric components
US10280622B2 (en) 2016-01-31 2019-05-07 Romeo Ilarian Ciuperca Self-annealing concrete forms and method of making and using same
JP6441298B2 (en) * 2016-03-24 2018-12-19 サン−ゴバン パフォーマンス プラスティックス コーポレイション Printable fabric
US20200389948A1 (en) * 2019-06-06 2020-12-10 Kenyon International, Inc. Cooktop Mat With Control Window
CN116814024B (en) * 2023-06-29 2023-12-15 扬州市岩特户外装备科技有限公司 Resin composite material and preparation method thereof

Citations (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3765932A (en) * 1969-12-10 1973-10-16 Shinko Pfaudler Method for anti-corrosive coating
US4210697A (en) * 1978-09-15 1980-07-01 Pall Corporation Process for preparing hydrophobic porous fibrous sheet material of high strength and porosity and product
US4298416A (en) * 1976-12-08 1981-11-03 Huron Chemicals Limited Protection of substrates against corrosion
US4339553A (en) * 1979-08-14 1982-07-13 Daikin Kogyo Co., Ltd. Water-based fluoroelastomer coating composition
US4347268A (en) * 1980-08-18 1982-08-31 David Hudson, Inc. Novel fluoroelastomer film compositions containing vinyl copolymers and method for the preparation thereof
US4370376A (en) * 1980-04-18 1983-01-25 E. I. Du Pont De Nemours And Company Tetrafluoroethylene polymer dispersions
US4503179A (en) * 1981-02-13 1985-03-05 Daikin Kogyo Co., Ltd. Aqueous fluorine-containing rubber coating composition and article coated therewith
US4504528A (en) * 1983-07-11 1985-03-12 Rm Industrial Products Company, Inc. Process for coating aqueous fluoropolymer coating on porous substrate
US4962136A (en) * 1984-08-17 1990-10-09 Alphaflex Industries, Inc. Elastomer-PTFE compositions, additives, and manufacturing methods
US5182151A (en) * 1989-07-10 1993-01-26 Sumitomo Chemical Company, Limited Thermoplastic resin composition
US5194335A (en) * 1984-04-13 1993-03-16 Chemical Fabrics Corporation Fluoropolymer coating and casting compositions and films derived therefrom
US5230937A (en) * 1983-04-13 1993-07-27 Chemfab Corporation Reinforced fluoropolymer composite
US5368924A (en) * 1992-05-22 1994-11-29 Alliedsignal Inc. Antenna cover fabric for microwave transmissive emitters
US5720703A (en) * 1996-06-28 1998-02-24 Eastman Kodak Company Amorphous fluoropolymer coated fusing member
US6133373A (en) * 1998-12-21 2000-10-17 Lauren International, Inc. Water-borne fluoroelastomer coatings and cured films therefrom
US6169139B1 (en) * 1998-04-27 2001-01-02 Dupont Dow Elastomers Llc Fluoroelastomer latex
US6379806B1 (en) * 1999-07-07 2002-04-30 Shin-Etsu Chemical Co., Ltd. Heat-resistant silicone rubber composite sheet having thermal conductivity and method of producing the same
US20020193500A1 (en) * 2000-04-14 2002-12-19 Klaus Hintzer Method of Making An Aqueous Dispersion of Fluoropolymers
US6664336B1 (en) * 1999-03-10 2003-12-16 Daikin Industries, Ltd. Aqueous curing composition of fluoroelastomer and article coated with fluoroelastomer
US6720381B1 (en) * 1999-10-05 2004-04-13 Daikin Industries, Ltd. Water-based composition for fluororubber vulcanization and article coated with fluororubber
US6764763B1 (en) * 1998-01-06 2004-07-20 Daikin Industries Ltd. Water-based vulcanizable fluororubber composition and coated article
US20040229043A1 (en) * 2003-05-13 2004-11-18 Spohn Peter D. Multilayer composite and method of making same
US20050001351A1 (en) * 2001-09-28 2005-01-06 Akira Yoshida Cushioning material for hot pressing and process for producing the same
US6930063B2 (en) * 2000-01-19 2005-08-16 Saint-Gobain Performance Plastics Corporation Non-curling reinforced composite membranes with differing opposed faces, methods for producing and their use in varied applications
US20050282023A1 (en) * 2000-01-19 2005-12-22 Saint-Gobain Performance Plastics Corporation Low coefficient of friction polymer film
US20060084743A1 (en) * 2004-10-20 2006-04-20 Chen John C Composition comprising polymer and silicone rubber
US20060122325A1 (en) * 2002-11-29 2006-06-08 Eckhard Wenz Blends having improved properties
US7238102B2 (en) * 2003-02-18 2007-07-03 Delphi Technologies, Inc. Heating, ventilation, and air conditioning system having a film valve and film for controlling air flow
US7247673B2 (en) * 2003-04-30 2007-07-24 National Starch And Chemical Investment Holding Corporation Waterbased high abrasion resistant coating
US7271209B2 (en) * 2002-08-12 2007-09-18 Exxonmobil Chemical Patents Inc. Fibers and nonwovens from plasticized polyolefin compositions
US7407899B2 (en) * 2003-01-10 2008-08-05 Milliken & Company Textile substrates having layered finish structure for improving liquid repellency and stain release
US7485588B2 (en) * 2003-01-10 2009-02-03 Yunzhang Wang Method for making textile substrates having layered finish structure for improving liquid repellency and stain release
US20090042038A1 (en) * 2006-04-05 2009-02-12 Asahi Glass Company, Limited Release film, releasable cushion material and process for producing printed board
US7547745B2 (en) * 2002-11-26 2009-06-16 Dow Global Technologies, Inc. Epoxy resin hardener of anhydride copolymer and anhydride-elastomer copolymer
US7803855B2 (en) * 2005-06-03 2010-09-28 Hexion Specialty Chemicals, Inc. Wood composites, methods of production, and methods of manufacture thereof

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB997096A (en) 1961-09-07 1965-06-30 Minnesota Mining & Mfg Polyblends of polytetrafluoroethylene and fluorocarbon elastomer latices
JPS4817545B1 (en) * 1969-02-26 1973-05-30
US3790403A (en) * 1972-01-13 1974-02-05 Du Pont Glass fabric coated with crack-free fluorocarbon resin coating and process for preparing
US3843386A (en) 1972-01-13 1974-10-22 Du Pont Coating of glass fabric coated with aqueous dispersion of polymer
US4532054A (en) * 1982-12-28 1985-07-30 General Electric Company Polyetherimide bearing compositions
DE125955T1 (en) * 1983-04-13 1985-06-05 Chemical Fabrics Corp., North Bennington, Vt. REINFORCED MULTILAYERED FLUOROPOLY MATERIAL AND METHOD FOR THE PRODUCTION THEREOF.
US4770927A (en) * 1983-04-13 1988-09-13 Chemical Fabrics Corporation Reinforced fluoropolymer composite
JPS60149452A (en) * 1984-01-17 1985-08-06 株式会社興人 Oil-resisting laminated sheet
JPS6134032A (en) * 1984-07-25 1986-02-18 Daikin Ind Ltd Coating fluororesin composition
DE3506524A1 (en) * 1985-02-25 1986-08-28 Akzo Gmbh, 5600 Wuppertal FLEXIBLE POLYIMIDE MULTILAYER LAMINATES
GB8913628D0 (en) 1989-06-14 1989-08-02 Courtaulds Plc Flexible coated substrate
JPH05177768A (en) * 1991-12-30 1993-07-20 Sumitomo Electric Ind Ltd Fluoroplastic coated article
GB9423138D0 (en) * 1994-11-16 1995-01-04 Scapa Group Plc Transfer printing and laminating blanket
US5947918A (en) 1996-11-18 1999-09-07 Gore Enterprise Holdings, Inc. Impact energy absorbing composite materials
EP1138718A1 (en) 1998-10-13 2001-10-04 Daikin Industries, Ltd. Aqueous composition for vulcanization of fluoro rubber and article coated with fluoro rubber
JP2001315248A (en) 2000-05-01 2001-11-13 Chuko Kasei Kogyo Kk Composite sheet
JP2002086616A (en) * 2000-09-18 2002-03-26 Nitto Denko Corp Glass fiber composite sheet and pressure-sensitive adhesive tape using the same
RU2213596C1 (en) * 2002-10-28 2003-10-10 Закрытое акционерное общество "Элиот" Protective outfit for firemen
US20070298231A1 (en) 2004-09-07 2007-12-27 Teijin Limited Transparent Conductive Laminated Body And Transparent Touch Panel
US7754795B2 (en) 2006-05-25 2010-07-13 3M Innovative Properties Company Coating composition
US7875563B2 (en) * 2007-03-28 2011-01-25 Honeywell International Inc. Method to create an environmentally resistant soft armor composite

Patent Citations (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3765932A (en) * 1969-12-10 1973-10-16 Shinko Pfaudler Method for anti-corrosive coating
US4298416A (en) * 1976-12-08 1981-11-03 Huron Chemicals Limited Protection of substrates against corrosion
US4210697A (en) * 1978-09-15 1980-07-01 Pall Corporation Process for preparing hydrophobic porous fibrous sheet material of high strength and porosity and product
US4339553A (en) * 1979-08-14 1982-07-13 Daikin Kogyo Co., Ltd. Water-based fluoroelastomer coating composition
US4370376A (en) * 1980-04-18 1983-01-25 E. I. Du Pont De Nemours And Company Tetrafluoroethylene polymer dispersions
US4347268A (en) * 1980-08-18 1982-08-31 David Hudson, Inc. Novel fluoroelastomer film compositions containing vinyl copolymers and method for the preparation thereof
US4503179A (en) * 1981-02-13 1985-03-05 Daikin Kogyo Co., Ltd. Aqueous fluorine-containing rubber coating composition and article coated therewith
US5230937A (en) * 1983-04-13 1993-07-27 Chemfab Corporation Reinforced fluoropolymer composite
US4504528A (en) * 1983-07-11 1985-03-12 Rm Industrial Products Company, Inc. Process for coating aqueous fluoropolymer coating on porous substrate
US5194335A (en) * 1984-04-13 1993-03-16 Chemical Fabrics Corporation Fluoropolymer coating and casting compositions and films derived therefrom
US4962136A (en) * 1984-08-17 1990-10-09 Alphaflex Industries, Inc. Elastomer-PTFE compositions, additives, and manufacturing methods
US5182151A (en) * 1989-07-10 1993-01-26 Sumitomo Chemical Company, Limited Thermoplastic resin composition
US5368924A (en) * 1992-05-22 1994-11-29 Alliedsignal Inc. Antenna cover fabric for microwave transmissive emitters
US5720703A (en) * 1996-06-28 1998-02-24 Eastman Kodak Company Amorphous fluoropolymer coated fusing member
US20040214944A1 (en) * 1998-01-06 2004-10-28 Daikin Industries, Ltd. Aqueous fluoroelastomer curable composition and coated article
US6764763B1 (en) * 1998-01-06 2004-07-20 Daikin Industries Ltd. Water-based vulcanizable fluororubber composition and coated article
US6169139B1 (en) * 1998-04-27 2001-01-02 Dupont Dow Elastomers Llc Fluoroelastomer latex
US6133373A (en) * 1998-12-21 2000-10-17 Lauren International, Inc. Water-borne fluoroelastomer coatings and cured films therefrom
US6664336B1 (en) * 1999-03-10 2003-12-16 Daikin Industries, Ltd. Aqueous curing composition of fluoroelastomer and article coated with fluoroelastomer
US6379806B1 (en) * 1999-07-07 2002-04-30 Shin-Etsu Chemical Co., Ltd. Heat-resistant silicone rubber composite sheet having thermal conductivity and method of producing the same
US6720381B1 (en) * 1999-10-05 2004-04-13 Daikin Industries, Ltd. Water-based composition for fluororubber vulcanization and article coated with fluororubber
US6930063B2 (en) * 2000-01-19 2005-08-16 Saint-Gobain Performance Plastics Corporation Non-curling reinforced composite membranes with differing opposed faces, methods for producing and their use in varied applications
US20050282023A1 (en) * 2000-01-19 2005-12-22 Saint-Gobain Performance Plastics Corporation Low coefficient of friction polymer film
US6794550B2 (en) * 2000-04-14 2004-09-21 3M Innovative Properties Company Method of making an aqueous dispersion of fluoropolymers
US20020193500A1 (en) * 2000-04-14 2002-12-19 Klaus Hintzer Method of Making An Aqueous Dispersion of Fluoropolymers
US20050001351A1 (en) * 2001-09-28 2005-01-06 Akira Yoshida Cushioning material for hot pressing and process for producing the same
US7271209B2 (en) * 2002-08-12 2007-09-18 Exxonmobil Chemical Patents Inc. Fibers and nonwovens from plasticized polyolefin compositions
US7547745B2 (en) * 2002-11-26 2009-06-16 Dow Global Technologies, Inc. Epoxy resin hardener of anhydride copolymer and anhydride-elastomer copolymer
US20060122325A1 (en) * 2002-11-29 2006-06-08 Eckhard Wenz Blends having improved properties
US7485588B2 (en) * 2003-01-10 2009-02-03 Yunzhang Wang Method for making textile substrates having layered finish structure for improving liquid repellency and stain release
US7407899B2 (en) * 2003-01-10 2008-08-05 Milliken & Company Textile substrates having layered finish structure for improving liquid repellency and stain release
US7238102B2 (en) * 2003-02-18 2007-07-03 Delphi Technologies, Inc. Heating, ventilation, and air conditioning system having a film valve and film for controlling air flow
US7247673B2 (en) * 2003-04-30 2007-07-24 National Starch And Chemical Investment Holding Corporation Waterbased high abrasion resistant coating
US20040229043A1 (en) * 2003-05-13 2004-11-18 Spohn Peter D. Multilayer composite and method of making same
US20060084743A1 (en) * 2004-10-20 2006-04-20 Chen John C Composition comprising polymer and silicone rubber
US7803855B2 (en) * 2005-06-03 2010-09-28 Hexion Specialty Chemicals, Inc. Wood composites, methods of production, and methods of manufacture thereof
US20090042038A1 (en) * 2006-04-05 2009-02-12 Asahi Glass Company, Limited Release film, releasable cushion material and process for producing printed board

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100044382A1 (en) * 2008-08-22 2010-02-25 Saint-Gobain Performance Plastics Corporation Fluoropolymer coated article
US9314132B2 (en) 2009-12-18 2016-04-19 Saint-Gobain Per.Plastics Corporation Cooking release sheet materials and release surfaces
US8673449B2 (en) 2009-12-18 2014-03-18 Saint-Gobain Performance Plastics Corporation Cooking release sheet materials and release surfaces
US20110146501A1 (en) * 2009-12-18 2011-06-23 Saint-Gobain Performance Plastics Corporation Cooking release sheet materials and release surfaces
US10194528B2 (en) * 2011-05-06 2019-01-29 Guangdong Shengyi Sci. Tech Co., Ltd. Composite material, high-frequency circuit baseboard made therefrom and production method thereof
US20130337250A1 (en) * 2012-05-30 2013-12-19 Richard J. Austin Modified perfluoropolymer material
US9634214B2 (en) * 2012-11-05 2017-04-25 Ledengin, Inc. Graphite-containing substrates for LED packages
US20140124822A1 (en) * 2012-11-05 2014-05-08 Ledengin, Inc. Graphite-containing substrates for led packages
US20150307670A1 (en) * 2014-04-25 2015-10-29 Saint-Gobain Performance Plastics Corporation Thin low friction liners
WO2016057689A1 (en) * 2014-10-07 2016-04-14 Saint-Gobain Performance Plastics Corporation Strength retention fabric
US20160097155A1 (en) * 2014-10-07 2016-04-07 Saint-Gobain Performance Plastics Corporation Strength retention fabric
TWI631259B (en) * 2014-10-07 2018-08-01 聖高拜塑膠製品公司 Strength retention fabric and method for producing the same
US10626550B2 (en) * 2015-11-24 2020-04-21 Bose Corporation Water-resistant composition
WO2017143097A1 (en) * 2016-02-16 2017-08-24 Saint-Gobain Performance Plastics Corporation Composite and method for making
US11034129B2 (en) * 2016-02-16 2021-06-15 Saint-Gobain Performance Plastics Corporation Composite and method for making
EP3416826A4 (en) * 2016-02-16 2019-11-06 Saint-Gobain Performance Plastics Corporation Composite and method for making
WO2017165384A1 (en) * 2016-03-21 2017-09-28 Saint-Gobain Performance Plastics Corporation Architectural membrane
EP3433100A4 (en) * 2016-03-21 2020-07-22 Saint-Gobain Performance Plastics Corporation Architectural membrane
US10751973B2 (en) 2016-03-21 2020-08-25 Saint-Gobain Performance Plastics Corporation Architectural membrane
US20170274694A1 (en) * 2016-03-24 2017-09-28 Saint-Gobain Performance Plastics Corporation Printable fabric
US11174418B2 (en) * 2016-06-27 2021-11-16 William Marsh Rice University Fluorine and hydrogen-based adhesive compositions and methods of making the same
US20200123406A1 (en) * 2016-10-24 2020-04-23 Saint-Gobain Performance Plastics Corporation Polymer compositions, materials, and methods of making
US11230648B2 (en) 2016-10-24 2022-01-25 Saint-Gobain Performance Plastics Corporation Polymer compositions, materials, and methods of making
US11326025B2 (en) 2017-02-24 2022-05-10 Lg Chem, Ltd. Polyamideimide copolymer and polyamideimide film comprising the same

Also Published As

Publication number Publication date
CN102449061B (en) 2014-08-20
US20150299943A1 (en) 2015-10-22
RU2011126894A (en) 2013-01-27
JP2015037874A (en) 2015-02-26
CA2747723A1 (en) 2010-07-01
CN102449061A (en) 2012-05-09
EP2376571B1 (en) 2018-02-28
JP5612596B2 (en) 2014-10-22
JP2012511454A (en) 2012-05-24
WO2010075210A3 (en) 2010-10-14
MX2011006681A (en) 2011-07-12
WO2010075210A2 (en) 2010-07-01
EP2376571A4 (en) 2013-06-19
EP2376571A2 (en) 2011-10-19
US8969222B2 (en) 2015-03-03
TW201030207A (en) 2010-08-16
RU2486216C2 (en) 2013-06-27
CA2953354A1 (en) 2010-07-01
TWI410550B (en) 2013-10-01
CA2747723C (en) 2017-02-28

Similar Documents

Publication Publication Date Title
US8969222B2 (en) Modified perfluoropolymer sheet material and methods for making same
US4770927A (en) Reinforced fluoropolymer composite
US20130337250A1 (en) Modified perfluoropolymer material
KR101468890B1 (en) Cooking belt
WO2001053073A1 (en) Non-curling reinforced composite membranes with differing opposed faces, methods for producing and their use in varied applications
EP2244878A2 (en) Multi-layer article
EP0731935A1 (en) Composite release material for elastomeric rollers
JP6620157B2 (en) Strength retaining fabric
US20020123282A1 (en) Fluoropolymer composites
US7470453B1 (en) Method for forming flexible composites using polymer coating materials
KR102270374B1 (en) Polymer Compositions, Materials and Methods of Making
JPH0711581A (en) Heat-resistant releasing sheet and its production

Legal Events

Date Code Title Description
AS Assignment

Owner name: SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION,OHIO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KEESE, FRANK M.;PLEYDON, ROBERT G.;HARDY, ANNE B.;AND OTHERS;SIGNING DATES FROM 20100211 TO 20100311;REEL/FRAME:024069/0251

Owner name: SAINT-GOBAIN PERFORMANCE PLASTICS CORPORATION, OHI

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KEESE, FRANK M.;PLEYDON, ROBERT G.;HARDY, ANNE B.;AND OTHERS;SIGNING DATES FROM 20100211 TO 20100311;REEL/FRAME:024069/0251

STCF Information on status: patent grant

Free format text: PATENTED CASE

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 4TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1551); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 4

FEPP Fee payment procedure

Free format text: MAINTENANCE FEE REMINDER MAILED (ORIGINAL EVENT CODE: REM.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

LAPS Lapse for failure to pay maintenance fees

Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20230303